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| Boli A-Z | | 3mc Syndrome
3mc Syndrome 2
3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria, Type I
3-Methylglutaconic Aciduria, Type Iii
3-Methylglutaconic Aciduria, Type Iv
3-Methylglutaconic Aciduria, Type Ix
3-Methylglutaconic Aciduria, Type V
3-Methylglutaconic Aciduria, Type Viii
3-Methylglutaconic Aciduria with Cataracts, Neurologic Involvement, and Neutropenia
3q26 Microduplication Syndrome
9q33.3q34.11 Microdeletion Syndrome
Abducens Nerve Disease
Abetalipoproteinemia
Ablepharon-Macrostomia Syndrome
Abnormal Pupillary Function
Abnormal Retinal Correspondence
Abnormal Threshold of Rods
Accommodative Esotropia
Accommodative Spasm
Aceruloplasminemia
Achromatopsia
Achromatopsia 2
Achromatopsia 3
Achromatopsia 4
Achromatopsia 7
Acquired Color Blindness
Acquired Cutis Laxa
Acquired Night Blindness
Acquired Pseudoxanthoma Elasticum
Acquired Tear Duct Stenosis
Acrocephalopolydactylous Dysplasia
Acrofacial Dysostosis 1, Nager Type
Acute Annular Outer Retinopathy
Acute Canaliculitis
Acute Closed-Angle Glaucoma
Acute Conjunctivitis
Acute Contagious Conjunctivitis
Acute Dacryoadenitis
Acute Dacryocystitis
Acute Endophthalmitis
Acute Hydrops Keratoconus
Acute Inflammation of Lacrimal Passage
Acute Macular Neuroretinopathy
Acute Orbital Inflammation
Acute Retinal Necrosis Syndrome
Acute Retrobulbar Neuritis
Acute Zonal Occult Outer Retinopathy
Adamantinoma of Long Bones
Adie Pupil
Adult Krabbe Disease
Adult Syndrome
Agnosia
Aicardi Syndrome
Aicar Transformylase/imp Cyclohydrolase Deficiency
Alagille Syndrome 1
Alagille Syndrome 2
Aland Island Eye Disease
Albinism, Ocular, Type I
Albinism, Ocular, with Late-Onset Sensorineural Deafness
Albinism, Ocular, with Sensorineural Deafness
Albinism, Oculocutaneous, Type Ia
Albinism, Oculocutaneous, Type Ib
Albinism, Oculocutaneous, Type Ii
Albinism, Oculocutaneous, Type Iii
Albinism, Oculocutaneous, Type Iv
Albinism, Oculocutaneous, Type V
Albinism, Oculocutaneous, Type Vi
Albinism, Oculocutaneous, Type Vii
Alexander Disease
Al Gazali Khidr Prem Chandran Syndrome
Alkaptonuria
Allergic Conjunctivitis
Allergic Contact Dermatitis of Eyelid
Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Recessive
Alport Syndrome, X-Linked
Alstrom Syndrome
Alternating Esotropia
Alternating Exotropia
Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis
Amblyopia
Ametropic Amblyopia
Amyloidosis, Finnish Type
Anal Atresia, Hypospadias, and Penoscrotal Inversion
Anatomical Narrow Angle Borderline Glaucoma
Angelucci's Syndrome
Angioid Streaks
Angioid Streaks of Choroid
Angular Blepharoconjunctivitis
Aniridia 1
Aniridia 2
Aniridia 3
Aniridia and Absent Patella
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation
Aniseikonia
Anisometropia
Ankyloblepharon Filiforme Adnatum and Cleft Palate
Ankyloblepharon Filiforme Adnatum-Imperforate Anus Syndrome
Anterior Corneal Pigmentation
Anterior Dislocation of Lens
Anterior Optic Tract Meningioma
Anterior Scleritis
Anterior Segment Dysgenesis 1
Anterior Segment Dysgenesis 2
Anterior Segment Dysgenesis 3
Anterior Segment Dysgenesis 4
Anterior Segment Dysgenesis 5
Anterior Segment Dysgenesis 6
Anterior Segment Dysgenesis 7
Anterior Segment Dysgenesis 8
Anterior Uveitis
Apert Syndrome
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction
Aplasia of Lacrimal and Salivary Glands
Apraxia of Eyelid Opening
Aqueous Misdirection
Arcus Corneae
Argyll Robertson Pupil
Arteritic Anterior Ischemic Optic Neuropathy
Asthenopia
Astigmatism
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia
Ataxia-Oculomotor Apraxia 3
Ataxia-Oculomotor Apraxia 4
Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation
Ataxia-Telangiectasia
Ataxia-Telangiectasia-Like Disorder 1
Ataxia-Telangiectasia-Like Disorder 2
Atopic Keratoconjunctivitis
Atp6v0a2-Related Cutis Laxa
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects
Atypical Pantothenate Kinase-Associated Neurodegeneration
Auditory Neuropathy and Optic Atrophy
Autoimmune-Related Retinopathy and Optic Neuropathy
Autoinflammation, Lipodystrophy, and Dermatosis Syndrome
Autosomal Dominant Congenital Stationary Night Blindness
Autosomal Dominant Optic Atrophy and Peripheral Neuropathy
Autosomal Dominant Optic Atrophy, Classic Form
Autosomal Dominant Optic Atrophy Plus Syndrome
Autosomal Dominant Progressive External Ophthalmoplegia
Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome
Autosomal Recessive Congenital Stationary Night Blindness
Autosomal Recessive Cutis Laxa Type 2, Classic Type
Autosomal Recessive Isolated Optic Atrophy
Autosomal Recessive Leukoencephalopathy-Ischemic Stroke-Retinitis Pigmentosa Syndrome
Autosomal Recessive Malignant Osteopetrosis
Autosomal Recessive Nonsyndromic Congenital Nuclear Cataract
Autosomal Recessive Spastic Paraplegia Type 59
Autosomal Recessive Spastic Paraplegia Type 60
Autosomal Recessive Spastic Paraplegia Type 66
Autosomal Recessive Spastic Paraplegia Type 67
Autosomal Recessive Spastic Paraplegia Type 68
Autosomal Recessive Spastic Paraplegia Type 69
Autosomal Recessive Spastic Paraplegia Type 70
Autosomal Recessive Spastic Paraplegia Type 71
Autosomal Recessive Stickler Syndrome
Axenfeld-Rieger Syndrome
Axenfeld-Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome, Type 2
Axenfeld-Rieger Syndrome, Type 3
Ayme-Gripp Syndrome
Background Diabetic Retinopathy
Bacterial Conjunctivitis
Balint Syndrome
Barber-Say Syndrome
Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 1
Bardet-Biedl Syndrome 10
Bardet-Biedl Syndrome 11
Bardet-Biedl Syndrome 12
Bardet-Biedl Syndrome 13
Bardet-Biedl Syndrome 14
Bardet-Biedl Syndrome 15
Bardet-Biedl Syndrome 16
Bardet-Biedl Syndrome 17
Bardet-Biedl Syndrome 18
Bardet-Biedl Syndrome 19
Bardet-Biedl Syndrome 2
Bardet-Biedl Syndrome 20
Bardet-Biedl Syndrome 21
Bardet-Biedl Syndrome 3
Bardet-Biedl Syndrome 4
Bardet-Biedl Syndrome 5
Bardet-Biedl Syndrome 6
Bardet-Biedl Syndrome 7
Bardet-Biedl Syndrome 8
Bardet-Biedl Syndrome 9
Basal Cell Nevus Syndrome
Basal Laminar Drusen
Basel-Vanagaite-Smirin-Yosef Syndrome
Behcet Syndrome
Behr Syndrome
Berk-Tabatznik Syndrome
Bestrophinopathy
Bestrophinopathy, Autosomal Recessive
Bietti Crystalline Corneoretinal Dystrophy
Bilateral Acute Depigmentation of the Iris
Bilateral Meningioma of Optic Nerve
Binocular Vision Disease
Birdshot Chorioretinopathy
Blepharitis
Blepharochalasis
Blepharocheilodontic Syndrome 1
Blepharocheilodontic Syndrome 2
Blepharoconjunctivitis
Blepharophimosis
Blepharophimosis, Ptosis, and Epicanthus Inversus
Blepharophimosis with Ptosis, Syndactyly, and Short Stature
Blepharoptosis, Myopia, and Ectopia Lentis
Blepharospasm
Blepharospasm, Benign Essential
Blessig's Cysts
Blind Hypertensive Eye
Blind Hypotensive Eye
Blood Group, Globoside System
Blue Cone Monochromacy
Borderline Glaucoma
Borjeson-Forssman-Lehmann Syndrome
Bornholm Eye Disease
Bosch-Boonstra-Schaaf Optic Atrophy Syndrome
Bothnia Retinal Dystrophy
Bowman's Membrane Folds or Rupture
Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation
Brawny Scleritis
Brittle Cornea Syndrome 1
Brittle Cornea Syndrome 2
Brooke-Spiegler Syndrome
Brown's Tendon Sheath Syndrome
Bullous Keratopathy
Bullous Retinoschisis
Butterfly-Shaped Pigment Dystrophy
Cahmr Syndrome
Cancer-Associated Retinopathy
Cataract
Cataract 10, Multiple Types
Cataract 11, Multiple Types
Cataract 12, Multiple Types
Cataract 13 with Adult I Phenotype
Cataract 14, Multiple Types
Cataract 15, Multiple Types
Cataract 16, Multiple Types
Cataract 17, Multiple Types
Cataract 18
Cataract 19, Multiple Types
Cataract 1, Multiple Types
Cataract 20, Multiple Types
Cataract 21, Multiple Types
Cataract 22, Multiple Types
Cataract 23, Multiple Types
Cataract 24
Cataract 25
Cataract 26, Multiple Types
Cataract 27
Cataract 28
Cataract 29
Cataract 2, Multiple Types
Cataract 30
Cataract 30, Multiple Types
Cataract 31, Multiple Types
Cataract 32, Multiple Types
Cataract 33
Cataract 33, Multiple Types
Cataract 34, Multiple Types
Cataract 35
Cataract 36
Cataract 37
Cataract 38
Cataract 39, Multiple Types
Cataract 3, Multiple Types
Cataract 40
Cataract 41
Cataract 42
Cataract 43
Cataract 44
Cataract 45
Cataract 46, Juvenile-Onset
Cataract 47
Cataract 4, Multiple Types
Cataract 5, Multiple Types
Cataract 6, Multiple Types
Cataract 7
Cataract 8, Multiple Types
Cataract 9, Multiple Types
Cataract, Aberrant Oral Frenula, and Growth Retardation
Cataract, Age-Related Nuclear
Cataract Congenital Autosomal Dominant
Cataract-Glaucoma
Cataract-Intellectual Disability-Anal Atresia-Urinary Defects Syndrome
Cataract Microcornea Syndrome
Cataracts, Growth Hormone Deficiency, Sensory Neuropathy, Sensorineural Hearing Loss, and Skeletal Dysplasia
Cataract, Total Congenital
Cat Eye Syndrome
Cavitary Optic Disc Anomalies
Central Cloudy Dystrophy of Francois
Central Corneal Ulcer
Central Gyrate Choroidal Dystrophy
Central Pterygium
Central Retinal Artery Occlusion
Central Serous Chorioretinopathy
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, and Sensorineural Hearing Loss
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss
Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2
Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy
Cerebral Cavernous Malformation, Familial
Cerebral Cavernous Malformations
Cerebral Cavernous Malformations 2
Cerebral Cavernous Malformations 3
Cerebral Visual Impairment
Cerebroretinal Microangiopathy with Calcifications and Cysts 1
Cerebroretinal Microangiopathy with Calcifications and Cysts 2
Cerebrotendinous Xanthomatosis
Cerulean Cataract
Chanarin-Dorfman Syndrome
Charcot-Marie-Tooth Disease, X-Linked Dominant, 1
Charcot-Marie-Tooth Disease, X-Linked Dominant, 6
Charcot-Marie-Tooth Disease, X-Linked Recessive, 2
Charcot-Marie-Tooth Disease, X-Linked Recessive, 3
Charcot-Marie-Tooth Disease, X-Linked Recessive, 5
Char Syndrome
Chediak-Higashi Syndrome
Chiasmal Syndrome
Childhood Optic Nerve Glioma
Childhood Optic Tract Astrocytoma
Cholestasis with Gallstone, Ataxia, and Visual Disturbance
Chondrodysplasia Punctata 1, X-Linked
Chondrodysplasia Punctata 1, X-Linked Recessive
Chondrodysplasia Punctata 2, X-Linked
Chondrodysplasia Punctata 2, X-Linked Dominant
Chondroectodermal Dysplasia with Night Blindness
Chorioretinal Atrophy, Progressive Bifocal
Chorioretinal Scar
Chorioretinitis
Chorioretinopathy Dominant Form Microcephaly
Choroidal Dystrophy, Central Areolar, 1
Choroidal Dystrophy, Central Areolar 2
Choroidal Dystrophy, Central Areolar, 3
Choroid Disease
Choroid Epithelioid Cell Melanoma
Choroideremia
Choroideremia, Deafness, and Mental Retardation
Choroideremia Hypopituitarism
Choroiditis
Choroid Mixed Cell Melanoma
Choroid Necrotic Melanoma
Choroid Spindle Cell Melanoma
Chromosome 13q14 Deletion Syndrome
Chromosome 16p13.3 Deletion Syndrome, Proximal
Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb
Chromosome 18p Deletion Syndrome
Chromosome 18q Deletion Syndrome
Chromosome 2q24 Microdeletion Syndrome
Chromosome 5p Duplication
Chromosome 6pter-P24 Deletion Syndrome
Chromosome 9p Duplication
Chronic Canaliculitis
Chronic Closed-Angle Glaucoma
Chronic Conjunctivitis
Chronic Dacryoadenitis
Chronic Dacryocystitis
Chronic Endophthalmitis
Chronic Follicular Conjunctivitis
Chronic Granulomatous Disease
Chronic Inflammation of Lacrimal Passage
Chronic Lacrimal Gland Enlargement
Chronic Orbital Inflammation
Chronic Progressive External Ophthalmoplegia
Chronic Relapsing Inflammatory Optic Neuropathy
Cicatricial Ectropion
Cicatricial Entropion
Cicatricial Lagophthalmos
Cicatricial Pemphigoid
Ciliary Body Cancer
Ciliary Body Epithelioid Cell Melanoma
Ciliary Body Mixed Cell Melanoma
Ciliary Body Spindle Cell Melanoma
Cinca Syndrome
Classic Progressive Supranuclear Palsy Syndrome
Cleft Lip-Retinopathy Syndrome
Coats Disease
Cobblestone Retinal Degeneration
Cochleosaccular Degeneration with Progressive Cataracts
Cockayne Syndrome
Cockayne Syndrome a
Cockayne Syndrome B
Cockayne Syndrome Type I
Cockayne Syndrome Type Ii
Cockayne Syndrome Type Iii
Cogan-Reese Syndrome
Cogan Syndrome
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome
Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome
Coloboma, Ocular, Autosomal Dominant
Coloboma, Ocular, Autosomal Recessive
Coloboma of Eye Lens
Coloboma of Eyelid
Coloboma of Inferior Eyelid
Coloboma of Iris
Coloboma of Macula
Coloboma of Macula and Skeletal Anomalies
Coloboma of Macula with Type B Brachydactyly
Coloboma of Optic Nerve
Coloboma of Optic Papilla
Coloboma of Superior Eyelid
Colobomatous Microphthalmia
Color Blindness
Colorblindness, Partial, Protan Series
Color Vision Deficiency
Combined Hamartoma of the Retina and Retinal Pigment Epithelium
Combined Oxidative Phosphorylation Deficiency 18
Combined Oxidative Phosphorylation Deficiency 31
Combined Oxidative Phosphorylation Deficiency 7
Complete Cryptophthalmia
Cone Dystrophy
Cone-Rod Dystrophy 1
Cone-Rod Dystrophy 10
Cone-Rod Dystrophy 11
Cone-Rod Dystrophy 12
Cone-Rod Dystrophy 13
Cone-Rod Dystrophy 15
Cone-Rod Dystrophy 16
Cone-Rod Dystrophy 17
Cone-Rod Dystrophy 18
Cone-Rod Dystrophy 19
Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 20
Cone-Rod Dystrophy 3
Cone-Rod Dystrophy 5
Cone-Rod Dystrophy 6
Cone-Rod Dystrophy 7
Cone-Rod Dystrophy 8
Cone-Rod Dystrophy 9
Cone-Rod Dystrophy, X-Linked, 1
Cone-Rod Dystrophy, X-Linked, 2
Cone-Rod Dystrophy, X-Linked, 3
Congenital Abducens Nerve Palsy
Congenital Aphakia
Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome
Congenital Cataracts, Facial Dysmorphism, and Neuropathy
Congenital Cataracts, Hearing Loss, and Neurodegeneration
Congenital Corneal Opacities, Cornea Guttata, and Corectopia
Congenital Cornea Plana
Congenital Ectropion Uveae
Congenital Eyelid Retraction
Congenital Hereditary Endothelial Dystrophy Type I
Congenital Ichthyosiform Erythroderma
Congenital Labioscrotal Agenesis-Cerebellar Malformation-Corneal Dystrophy-Facial Dysmorphism Syndrome
Congenital Myasthenic Syndrome
Congenital Myasthenic Syndromes with Glycosylation Defect
Congenital Oculomotor Nerve Palsy
Congenital Ptosis
Congenital Retinal Arteriovenous Communication
Congenital Sialidosis Type 2
Congenital Stationary Night Blindness
Congenital Symblepharon
Congenital Trochlear Nerve Palsy
Conjugate Gaze Palsy
Conjunctival Concretion
Conjunctival Degeneration
Conjunctival Deposit
Conjunctival Disease
Conjunctival Folliculosis
Conjunctival Pigmentation
Conjunctival Vascular Disease
Conjunctivitis
Conjunctivitis with Pseudomembrane
Conjunctivochalasis
Constant Exophthalmos
Contact Blepharoconjunctivitis
Contact Lens Corneal Edema
Corneal Abscess
Corneal Argyrosis
Corneal Degeneration
Corneal Deposit
Corneal Disease
Corneal Dystrophy
Corneal Dystrophy and Perceptive Deafness
Corneal Dystrophy, Avellino Type
Corneal Dystrophy, Band-Shaped
Corneal Dystrophy, Congenital Stromal
Corneal Dystrophy, Endothelial, X-Linked
Corneal Dystrophy, Epithelial Basement Membrane
Corneal Dystrophy, Fleck
Corneal Dystrophy, Gelatinous Drop-Like
Corneal Dystrophy, Groenouw Type I
Corneal Dystrophy, Lattice Type I
Corneal Dystrophy, Lattice Type Iiia
Corneal Dystrophy, Lisch Epithelial
Corneal Dystrophy, Meesmann
Corneal Dystrophy, Posterior Amorphous
Corneal Dystrophy, Posterior Polymorphous, 1
Corneal Dystrophy, Posterior Polymorphous, 2
Corneal Dystrophy, Posterior Polymorphous, 3
Corneal Dystrophy, Reis-Bucklers Type
Corneal Dystrophy, Subepithelial Mucinous
Corneal Dystrophy, Thiel-Behnke Type
Corneal Ectasia
Corneal Edema
Corneal Endothelial Dystrophy
Corneal Endothelial Dystrophy Type 2
Corneal Granular Dystrophy
Corneal Hypesthesia, Familial
Corneal Neovascularization
Corneal Staphyloma
Corneal Ulcer
Cornea Plana
Cornea Plana 1, Autosomal Dominant
Cornea Plana 2, Autosomal Recessive
Cornelia De Lange Syndrome
Cornelia De Lange Syndrome 1
Cornelia De Lange Syndrome 2
Cornelia De Lange Syndrome 3
Cornelia De Lange Syndrome 4
Cornelia De Lange Syndrome 5
Corneodermatoosseous Syndrome
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia
Cortical Blindness
Cortical Blindness, Retardation, and Postaxial Polydactyly
Cortical Dysplasia, Complex, with Other Brain Malformations 8
Cortical Senile Cataract
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation
Crater-Like Holes of Optic Disc
Cri-Du-Chat Syndrome
Crouzon Syndrome
Crouzon Syndrome with Acanthosis Nigricans
Cryptophthalmos, Unilateral or Bilateral, Isolated
Cutis Laxa
Cutis Laxa, Autosomal Dominant 1
Cutis Laxa, Autosomal Dominant 2
Cutis Laxa, Autosomal Dominant 3
Cutis Laxa, Autosomal Recessive Type 1
Cutis Laxa, Autosomal Recessive, Type Ia
Cutis Laxa, Autosomal Recessive, Type Ib
Cutis Laxa, Autosomal Recessive, Type Ic
Cutis Laxa, Autosomal Recessive, Type Iia
Cutis Laxa, Autosomal Recessive, Type Iib
Cutis Laxa, Autosomal Recessive, Type Iic
Cutis Laxa, Autosomal Recessive, Type Iid
Cutis Laxa, Autosomal Recessive, Type Iiia
Cutis Laxa, Autosomal Recessive, Type Iiib
Cycloplegia
Cyclotropia
Cylindromatosis, Familial
Cystinosis, Adult Nonnephropathic
Cystoid Macular Retinal Degeneration
Cytomegalovirus Retinitis
Dacryoadenitis
Dacryocystitis
Dacryocystocele
Deafness and Myopia
De Barsy Syndrome
Deep Corneal Vascularisation
Deep Keratitis
Degeneration of Macula and Posterior Pole
Degenerative Myopia
Dermochondrocorneal Dystrophy
Dermoids of Cornea
Diabetes and Deafness, Maternally Inherited
Diabetic Cataract
Diabetic Macular Edema
Diffuse Interstitial Keratitis
Diffuse Secondary Choroid Atrophy
Discoid Lupus Erythematosus of Eyelid
Disseminated Chorioretinitis
Distal Trisomy 10q
Distal Trisomy 14q
Distal Trisomy 15q
Distal Trisomy 2p
Distichiasis
Disuse Amblyopia
Dopamine Beta-Hydroxylase Deficiency, Congenital
Double Pterygium
Doyne Honeycomb Retinal Dystrophy
Dry Eye Syndrome
Duane-Radial Ray Syndrome
Duane Retraction Syndrome
Duane Retraction Syndrome 1
Duane Retraction Syndrome 2
Dubowitz Syndrome
Dyskeratosis Congenita
Dyskeratosis Congenita Autosomal Dominant
Dyskeratosis Congenita, Autosomal Dominant 1
Dyskeratosis Congenita, Autosomal Dominant 2
Dyskeratosis Congenita, Autosomal Dominant 3
Dyskeratosis Congenita, Autosomal Dominant 6
Dyskeratosis Congenita Autosomal Recessive
Dyskeratosis Congenita, Autosomal Recessive 1
Dyskeratosis Congenita, Autosomal Recessive 2
Dyskeratosis Congenita, Autosomal Recessive 3
Dyskeratosis Congenita, Autosomal Recessive 5
Dyskeratosis Congenita, Autosomal Recessive 6
Dyskeratosis, Hereditary Benign Intraepithelial
Dyssegmental Dysplasia with Glaucoma
Dystonia, Childhood-Onset, with Optic Atrophy and Basal Ganglia Abnormalities
Dystrophies Primarily Involving the Retinal Pigment Epithelium
Eales Disease
Early-Onset Anterior Polar Cataract
Early-Onset Glaucoma
Early-Onset Non-Syndromic Cataract
Early-Onset Nuclear Cataract
Early-Onset Partial Cataract
Early-Onset Posterior Subcapsular Cataract
Early-Onset Progressive Diffuse Brain Atrophy-Microcephaly-Muscle Weakness-Optic Atrophy Syndrome
Early-Onset Zonular Cataract
Eccrine Syringofibroadenomatosis with Eyelid Abnormalities
Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant
Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive
Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant
Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive
Ectodermal Dysplasia 1, Hypohidrotic, X-Linked
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy Syndrome
Ectodermal Dysplasia/skin Fragility Syndrome
Ectopia Lentis 1, Isolated, Autosomal Dominant
Ectopia Lentis 2, Isolated, Autosomal Recessive
Ectropion
Eczema Herpeticum
Eczematous Dermatitis of Eyelid
Edict Syndrome
Encephalopathy
Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 1
Encephalopathy Due to Defective Mitochondrial and Peroxisomal Fission 2
Encephalopathy, Progressive, with Amyotrophy and Optic Atrophy
Endocrine Exophthalmos
Endophthalmitis
Endotheliitis
Enhanced S-Cone Syndrome
Enophthalmos
Enthesitis-Related Juvenile Idiopathic Arthritis
Entropion
Epiblepharon
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Dystrophica, Autosomal Dominant
Epidermolysis Bullosa Dystrophica, Autosomal Recessive
Epidermolysis Bullosa, Junctional, Herlitz Type
Epidermolysis Bullosa Simplex with Muscular Dystrophy
Epilepsy, Hearing Loss, and Mental Retardation Syndrome
Epileptic Encephalopathy, Early Infantile, 1
Epileptic Encephalopathy, Early Infantile, 11
Epileptic Encephalopathy, Early Infantile, 12
Epileptic Encephalopathy, Early Infantile, 13
Epileptic Encephalopathy, Early Infantile, 14
Epileptic Encephalopathy, Early Infantile, 15
Epileptic Encephalopathy, Early Infantile, 16
Epileptic Encephalopathy, Early Infantile, 17
Epileptic Encephalopathy, Early Infantile, 18
Epileptic Encephalopathy, Early Infantile, 19
Epileptic Encephalopathy, Early Infantile, 2
Epileptic Encephalopathy, Early Infantile, 21
Epileptic Encephalopathy, Early Infantile, 23
Epileptic Encephalopathy, Early Infantile, 24
Epileptic Encephalopathy, Early Infantile, 25
Epileptic Encephalopathy, Early Infantile, 26
Epileptic Encephalopathy, Early Infantile, 27
Epileptic Encephalopathy, Early Infantile, 28
Epileptic Encephalopathy, Early Infantile, 29
Epileptic Encephalopathy, Early Infantile, 3
Epileptic Encephalopathy, Early Infantile, 30
Epileptic Encephalopathy, Early Infantile, 31
Epileptic Encephalopathy, Early Infantile, 32
Epileptic Encephalopathy, Early Infantile, 33
Epileptic Encephalopathy, Early Infantile, 34
Epileptic Encephalopathy, Early Infantile, 35
Epileptic Encephalopathy, Early Infantile, 36
Epileptic Encephalopathy, Early Infantile, 37
Epileptic Encephalopathy, Early Infantile, 38
Epileptic Encephalopathy, Early Infantile, 39
Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 40
Epileptic Encephalopathy, Early Infantile, 41
Epileptic Encephalopathy, Early Infantile, 42
Epileptic Encephalopathy, Early Infantile, 43
Epileptic Encephalopathy, Early Infantile, 44
Epileptic Encephalopathy, Early Infantile, 45
Epileptic Encephalopathy, Early Infantile, 46
Epileptic Encephalopathy, Early Infantile, 47
Epileptic Encephalopathy, Early Infantile, 48
Epileptic Encephalopathy, Early Infantile, 49
Epileptic Encephalopathy, Early Infantile, 5
Epileptic Encephalopathy, Early Infantile, 50
Epileptic Encephalopathy, Early Infantile, 51
Epileptic Encephalopathy, Early Infantile, 52
Epileptic Encephalopathy, Early Infantile, 53
Epileptic Encephalopathy, Early Infantile, 54
Epileptic Encephalopathy, Early Infantile, 55
Epileptic Encephalopathy, Early Infantile, 56
Epileptic Encephalopathy, Early Infantile, 57
Epileptic Encephalopathy, Early Infantile, 58
Epileptic Encephalopathy, Early Infantile, 6
Epileptic Encephalopathy, Early Infantile, 7
Epileptic Encephalopathy, Early Infantile, 8
Epileptic Encephalopathy, Early Infantile, 9
Epiphora Due to Excess Lacrimation
Epiphora Due to Insufficient Drainage
Episcleritis Periodica Fugax
Epithelial and Subepithelial Dystrophy
Epithelial Basement Membrane Dystrophy
Epithelial Recurrent Erosion Dystrophy
Epithelial-Stromal Tgfbi Dystrophy
Equatorial Staphyloma
Erythrocyte Galactose Epimerase Deficiency
Esotropia
Essential Iris Atrophy
Euryblepharon
Euthyroid Graves Orbitopathy
Eversion of Lacrimal Punctum
Ewing Sarcoma
Excessive Tearing
Exfoliation Syndrome
Exophthalmic Ophthalmoplegia
Exophthalmos
Exotropia
Exposure Keratitis
Extensive Peripapillary Myelinated Nerve Fibers
Exudative Vitreoretinopathy
Exudative Vitreoretinopathy 1
Exudative Vitreoretinopathy 3
Exudative Vitreoretinopathy 4
Exudative Vitreoretinopathy 5
Exudative Vitreoretinopathy 6
Exudative Vitreoretinopathy 7
Eye Accommodation Disease
Eyebrows, Duplication of, with Stretchable Skin and Syndactyly
Eyebrow, Whorl in
Eye Degenerative Disease
Eyelid Degenerative Disease
Eyelid Disease
Eyelid Neoplasm
Fabry Disease
Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, and Spontaneous Filtering Blebs
Familial Adenomatous Polyposis
Familial Adenomatous Polyposis 1
Familial Adenomatous Polyposis 2
Familial Adenomatous Polyposis 3
Familial Adenomatous Polyposis 4
Familial Amyloidosis, Finnish Type
Familial Drusen
Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland
Familial Keratoacanthoma
Familial Monosomy 7 Syndrome
Familial Porphyria Cutanea Tarda
Familial Retinoblastoma
Familial Short Qt Syndrome
Farber Lipogranulomatosis
Filamentary Keratitis
Filarial Elephantiasis
Fish-Eye Disease
Flat Retinoschisis
Fleck Retina, Familial Benign
Fleck Retina of Kandori
Focal Chorioretinitis
Focal Dermal Hypoplasia
Form Agnosia
Foster-Kennedy Syndrome
Fourth Cranial Nerve Palsy
Fourth Cranial Nerve Palsy, Familial Congenital
Foveal Hypoplasia 1
Foveal Hypoplasia 2
Fragile X Syndrome
Fragile X Syndrome Type 1
Fragile X Syndrome Type 2
Fragile X Syndrome Type 3
Fraser-Like Syndrome
Fraser Syndrome 1
Fraser Syndrome 2
Fraser Syndrome 3
Friedreich Ataxia 1
Friedreich Ataxia 2
Friedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness
Frontofacionasal Dysplasia
Fuchs' Endothelial Dystrophy
Fuchs' Heterochromic Uveitis
Fucosidosis
Fucosidosis Type 1
Fundus Albipunctatus
Fundus Dystrophy
Fundus Pulverulentus
Galactokinase Deficiency
Galactose Epimerase Deficiency
Galactosemia
Galactosialidosis
Galloway-Mowat Syndrome
Galloway-Mowat Syndrome 1
Galloway-Mowat Syndrome 3
Galloway-Mowat Syndrome 4
Galloway-Mowat Syndrome 5
Gangliosidosis Gm1
Gangliosidosis Gm2
Gapo Syndrome
Gaucher's Disease
Gaucher Disease, Type I
Gaucher Disease, Type Ii
Gaucher Disease, Type Iii
Gaucher Disease, Type Iiic
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 1
Generalized Galactose Epimerase Deficiency
Giant Papillary Conjunctivitis
Gillespie Syndrome
Glaucoma 1, Open Angle, a
Glaucoma 1, Open Angle, I
Glaucoma 1, Open Angle, P
Glaucoma 3, Primary Congenital, a
Glaucoma 3, Primary Congenital, C
Glaucoma 3, Primary Congenital, D
Glaucoma 3, Primary Congenital, E
Glaucoma 3, Primary Infantile, B
Glaucoma and Sleep Apnea
Glaucoma, Hereditary
Glaucoma, Hereditary Adult Type 1a
Glaucoma, Hereditary Juvenile Type 1b
Glaucoma, Primary Infantile Type 3a
Glaucoma, Primary Open Angle
Glaucoma-Related Pigment Dispersion Syndrome
Glaucomatocyclitic Crisis
Glaucomatous Atrophy of Optic Disc
Glaucoma Type 1c
Gm1-Gangliosidosis, Type I
Gm1-Gangliosidosis, Type Ii
Gm1-Gangliosidosis, Type Iii
Gm2 Gangliosidosis, 0 Variant
Gm2-Gangliosidosis, Ab Variant
Gm2-Gangliosidosis, B, B1, Ab Variant
Gms Syndrome
Goldberg-Shprintzen Syndrome
Gonococcal Endophthalmia
Gonococcal Iridocyclitis
Gonococcal Keratitis
Granulomatous Disease, Chronic, Autosomal Dominant Type
Grayson-Wilbrandt Corneal Dystrophy
Griscelli Syndrome
Griscelli Syndrome, Type 1
Griscelli Syndrome, Type 2
Griscelli Syndrome, Type 3
Grouped Pigmentation of the Retina
Growth Retardation Alopecia Pseudoanodontia Optic
Gyrate Atrophy of Choroid and Retina
Hallermann-Streiff-Like Syndrome
Hallermann-Streiff Syndrome
Hemifacial Microsomia
Hereditary Choroidal Atrophy
Hereditary Hemorrhagic Telangiectasia
Hereditary Motor and Sensory Neuropathy, Type Iic
Hereditary Motor and Sensory Neuropathy V
Hereditary Night Blindness
Hereditary Retinal Dystrophy
Hereditary Sensory and Autonomic Neuropathy Type 1e
Hereditary Spastic Paraplegia
Hereditary Spastic Paraplegia 51
Hereditary Spastic Paraplegia 72
Hermansky-Pudlak Syndrome
Hermansky-Pudlak Syndrome 1
Hermansky-Pudlak Syndrome 10
Hermansky-Pudlak Syndrome 2
Hermansky-Pudlak Syndrome 3
Hermansky-Pudlak Syndrome 4
Hermansky-Pudlak Syndrome 5
Hermansky-Pudlak Syndrome 6
Hermansky-Pudlak Syndrome 7
Hermansky-Pudlak Syndrome 8
Hermansky-Pudlak Syndrome 9
Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis
Hermansky-Pudlak Syndrome with Pulmonary Fibrosis
Herpes Simplex Virus Keratitis
Histoplasmosis Retinitis
Hole Retinal Cyst
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency
Honey-Droplet Corneal Dystrophy
Hordeolum
Hordeolum Externum
Horner's Syndrome
Horner Syndrome, Congenital
Hurler-Scheie Syndrome
Hurler Syndrome
Hydrophthalmos
Hyperferritinemia with or Without Cataract
Hyperpigmentation of Eyelids
Hypersecretion Glaucoma
Hypertensive Retinopathy
Hypertrichosis Lanuginosa Congenita
Hypertrichosis of Eyelid
Hypertrichosis Universalis Congenita, Ambras Type
Hypertropia
Hypogonadism-Cataract Syndrome
Hypogonadotropic Hypogonadism-Retinitis Pigmentosa Syndrome
Hypohidrotic Ectodermal Dysplasia Autosomal Recessive
Hypomagnesemia 5, Renal, with Ocular Involvement
Hypomelanosis of Ito
Hypomyelinating Leukodystrophy
Hypoparathyroidism, Familial Isolated
Hypopigmentation of Eyelid
Hypopyon
Hypopyon Ulcer
Hypotonia, Infantile, with Psychomotor Retardation
Hypotrichosis, Congenital, with Juvenile Macular Dystrophy
Hypotrichosis of Eyelid
Hypotropia
Ichthyosis--Cheek--Eyebrow Syndrome
Ichthyosis, X-Linked
Idiopathic Anterior Uveitis
Idiopathic Corneal Edema
Idiopathic Linear Interstitial Keratitis
Idiopathic Macular Telangiectasia Type 1
Idiopathic Macular Telangiectasia Type 3
Idiopathic Panuveitis
Idiopathic Posterior Uveitis
Idiopathic Uveal Effusion Syndrome
Igg4-Related Ophthalmic Disease
Immature Cataract
Incontinentia Pigmenti
Infantile Cerebellar-Retinal Degeneration
Infantile Epileptic Encephalopathy
Infantile Krabbe Disease
Infantile-Onset Axonal Motor and Sensory Neuropathy-Optic Atrophy-Neurodegenerative Syndrome
Infectious Anterior Uveitis
Infectious Epithelial Keratitis
Infectious Panuveitis
Infectious Posterior Uveitis
Intellectual Disability-Cataracts-Kyphosis Syndrome
Intermediate Cell Type Ciliary Body Melanoma
Intermediate Uveitis
Intermittent Proptosis
Intermittent Squint
Internal Hordeolum
Internuclear Ophthalmoplegia
Interstitial Keratitis
Interval Angle-Closure Glaucoma
Intraocular Lymphoma
Intraocular Medulloepithelioma
Intraocular Pressure Quantitative Trait Locus
Inverse Marcus-Gunn Phenomenon
Iridocorneal Endothelial Syndrome
Iridocyclitis
Iris Disease
Iris Mixed Cell Melanoma
Iris Spindle Cell Melanoma
Iritis
Irregular Astigmatism
Irvan Syndrome
Ischemic Optic Neuropathy
Isolated Aniridia
Isolated Ankyloblepharon Filiforme Adnatum
Isolated Brachycephaly
Isolated Congenital Alacrima
Isolated Congenital Ectropion
Isolated Congenital Megalocornea
Isolated Ectopia Lentis
Isolated Optic Neuritis
Isolated Oxycephaly
Isolated Plagiocephaly
Isolated Scaphocephaly
Isolated Trigonocephaly
Jacobsen Syndrome
Jeavons Syndrome
Jorgenson Lenz Syndrome
Joubert Syndrome with Ocular Anomalies
Joubert Syndrome with Oculorenal Anomalies
Juvenile Glaucoma
Juvenile Sialidosis Type 2
Kabuki Syndrome 1
Kabuki Syndrome 2
Kearns-Sayre Syndrome
Keratitis, Hereditary
Keratoacanthoma
Keratoconjunctivitis
Keratoconjunctivitis Sicca
Keratoconus
Keratoconus 1
Keratoconus 2
Keratoconus 3
Keratoconus 4
Keratoconus 5
Keratoconus 6
Keratoconus 7
Keratoconus 8
Keratomalacia
Keratopathy
Keratosis Follicularis Spinulosa Decalvans
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
Kid Syndrome
Kluver-Bucy Syndrome
Knobloch Syndrome
Knobloch Syndrome 1
Krabbe Disease
Kufor-Rakeb Syndrome
Kuhnt-Junius Degeneration
Lacrimal Apparatus Disease
Lacrimal Duct Defect
Lacrimal Duct Obstruction
Lacrimal Passage Granuloma
Lacrimoauriculodentodigital Syndrome
Lagophthalmos
Laryngoonychocutaneous Syndrome
Late-Infantile/juvenile Krabbe Disease
Late-Onset Retinal Degeneration
Late-Onset Retinal Degenration
Lateral Displacement of Eye
Lattice Corneal Dystrophy
Lattice Corneal Dystrophy Type Ii
Lattice Degeneration of Retina Leading to Retinal Detachment
Laurence-Moon Syndrome
Leber Congenital Amaurosis
Leber Congenital Amaurosis 1
Leber Congenital Amaurosis 10
Leber Congenital Amaurosis 11
Leber Congenital Amaurosis 12
Leber Congenital Amaurosis 13
Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 15
Leber Congenital Amaurosis 16
Leber Congenital Amaurosis 17
Leber Congenital Amaurosis 2
Leber Congenital Amaurosis 3
Leber Congenital Amaurosis 4
Leber Congenital Amaurosis 5
Leber Congenital Amaurosis 6
Leber Congenital Amaurosis 7
Leber Congenital Amaurosis 8
Leber Congenital Amaurosis 9
Leber Hereditary Optic Neuropathy
Leber Optic Atrophy
Leber Optic Atrophy and Dystonia
Lecithin:cholesterol Acyltransferase Deficiency
Leigh Syndrome
Leigh Syndrome, French Canadian Type
Leigh Syndrome with Leukodystrophy
Leigh Syndrome with Nephrotic Syndrome
Lens Disease
Lens-Induced Iridocyclitis
Lens Subluxation
Leukocoria
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
Leukodystrophy, Hypomyelinating, 10
Leukodystrophy, Hypomyelinating, 11
Leukodystrophy, Hypomyelinating, 12
Leukodystrophy, Hypomyelinating, 13
Leukodystrophy, Hypomyelinating, 2
Leukodystrophy, Hypomyelinating, 3
Leukodystrophy, Hypomyelinating, 4
Leukodystrophy, Hypomyelinating, 5
Leukodystrophy, Hypomyelinating, 6
Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism
Leukodystrophy, Hypomyelinating, 9
Limb-Mammary Syndrome
Linear Skin Defects with Multiple Congenital Anomalies 1
Linear Skin Defects with Multiple Congenital Anomalies 2
Linear Skin Defects with Multiple Congenital Anomalies 3
Localized Anterior Staphyloma
Loeys-Dietz Syndrome 2
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Lopes Gorlin Syndrome
Lowe Oculocerebrorenal Syndrome
Lowry-Maclean Syndrome
Low Tension Glaucoma
Luxation of Globe
Macrophthalmia, Colobomatous, with Microcornea
Macular Degeneration, Age-Related, 1
Macular Degeneration, Age-Related, 10
Macular Degeneration, Age-Related, 11
Macular Degeneration, Age-Related, 12
Macular Degeneration, Age-Related, 13
Macular Degeneration, Age-Related, 14
Macular Degeneration, Age-Related, 15
Macular Degeneration, Age-Related, 2
Macular Degeneration, Age-Related, 4
Macular Degeneration, Age-Related, 5
Macular Degeneration, Age-Related, 6
Macular Degeneration, Age-Related, 7
Macular Degeneration, Age-Related, 8
Macular Degeneration, Age-Related, 9
Macular Degeneration, Early-Onset
Macular Dystrophy, Concentric Annular
Macular Dystrophy, Corneal
Macular Dystrophy, Dominant Cystoid
Macular Dystrophy, Patterned, 1
Macular Dystrophy, Patterned, 2
Macular Dystrophy, Patterned, 3
Macular Dystrophy, Retinal, 1, North Carolina Type
Macular Dystrophy, Retinal, 2
Macular Dystrophy, Retinal, 3
Macular Dystrophy, Vitelliform, 1
Macular Dystrophy, Vitelliform, 2
Macular Dystrophy, Vitelliform, 3
Macular Dystrophy, Vitelliform, 4
Macular Dystrophy, Vitelliform, 5
Macular Holes
Macular Keratitis
Macular Retinal Edema
Malignant Choroid Melanoma
Malignant Ciliary Body Melanoma
Malignant Eyelid Melanoma
Malignant Iris Melanoma
Manitoba Oculotrichoanal Syndrome
Mannosidosis, Alpha B, Lysosomal
Mannosidosis, Beta a, Lysosomal
Marcus Gunn Phenomenon
Marfan Syndrome
Marginal Corneal Ulcer
Marin-Amat Syndrome
Marinesco-Sjogren-Like Syndrome
Marinesco-Sjogren Syndrome
Marshall Syndrome
Martsolf Syndrome
Maternally-Inherited Progressive External Ophthalmoplegia
Mature Cataract
Mechanical Ectropion
Mechanical Entropion
Mechanical Lagophthalmos
Mechanical Strabismus
Meckel Syndrome 12
Meckel Syndrome 13
Meckel Syndrome, Type 1
Meckel Syndrome, Type 10
Meckel Syndrome, Type 11
Meckel Syndrome, Type 2
Meckel Syndrome, Type 3
Meckel Syndrome, Type 4
Meckel Syndrome, Type 5
Meckel Syndrome, Type 6
Meckel Syndrome, Type 7
Meckel Syndrome, Type 8
Meckel Syndrome, Type 9
Megalocornea
Megalocornea-Mental Retardation Syndrome
Meibomian Cyst
Melanoma, Cutaneous Malignant 1
Melanoma, Cutaneous Malignant 10
Melanoma, Cutaneous Malignant 2
Melanoma, Cutaneous Malignant 3
Melanoma, Cutaneous Malignant 4
Melanoma, Cutaneous Malignant 5
Melanoma, Cutaneous Malignant 6
Melanoma, Cutaneous Malignant 7
Melanoma, Cutaneous Malignant 8
Melanoma, Cutaneous Malignant 9
Melanoma, Uveal
Melanoma, Uveal 1
Melanoma, Uveal 2
Melnick-Needles Syndrome
Menkes Disease
Mental Retardation, Autosomal Dominant 10
Mental Retardation, Autosomal Dominant 11
Mental Retardation, Autosomal Dominant 13
Mental Retardation, Autosomal Dominant 18
Mental Retardation, Autosomal Dominant 19
Mental Retardation, Autosomal Dominant 20
Mental Retardation, Autosomal Dominant 21
Mental Retardation, Autosomal Dominant 22
Mental Retardation, Autosomal Dominant 23
Mental Retardation, Autosomal Dominant 24
Mental Retardation, Autosomal Dominant 26
Mental Retardation, Autosomal Dominant 27
Mental Retardation, Autosomal Dominant 29
Mental Retardation, Autosomal Dominant 30
Mental Retardation, Autosomal Dominant 31
Mental Retardation, Autosomal Dominant 32
Mental Retardation, Autosomal Dominant 33
Mental Retardation, Autosomal Dominant 34
Mental Retardation, Autosomal Dominant 35
Mental Retardation, Autosomal Dominant 36
Mental Retardation, Autosomal Dominant 38
Mental Retardation, Autosomal Dominant 39
Mental Retardation, Autosomal Dominant 40
Mental Retardation, Autosomal Dominant 41
Mental Retardation, Autosomal Dominant 42
Mental Retardation, Autosomal Dominant 43
Mental Retardation, Autosomal Dominant 44
Mental Retardation, Autosomal Dominant 45
Mental Retardation, Autosomal Dominant 46
Mental Retardation, Autosomal Dominant 47
Mental Retardation, Autosomal Dominant 48
Mental Retardation, Autosomal Dominant 49
Mental Retardation, Autosomal Dominant 50
Mental Retardation, Autosomal Dominant 51
Mental Retardation, Autosomal Dominant 52
Mental Retardation, Autosomal Dominant 53
Mental Retardation, Autosomal Dominant 54
Mental Retardation, Autosomal Dominant 56
Mental Retardation, Autosomal Dominant 7
Mental Retardation, Autosomal Recessive 14
Mental Retardation, Autosomal Recessive 15
Mental Retardation, Autosomal Recessive 16
Mental Retardation, Autosomal Recessive 18
Mental Retardation, Autosomal Recessive 19
Mental Retardation, Autosomal Recessive 2
Mental Retardation, Autosomal Recessive 23
Mental Retardation, Autosomal Recessive 24
Mental Retardation, Autosomal Recessive 25
Mental Retardation, Autosomal Recessive 27
Mental Retardation, Autosomal Recessive 28
Mental Retardation, Autosomal Recessive 29
Mental Retardation, Autosomal Recessive 30
Mental Retardation, Autosomal Recessive 31
Mental Retardation, Autosomal Recessive 33
Mental Retardation, Autosomal Recessive 35
Mental Retardation, Autosomal Recessive 36
Mental Retardation, Autosomal Recessive 37
Mental Retardation, Autosomal Recessive 38
Mental Retardation, Autosomal Recessive 39
Mental Retardation, Autosomal Recessive 40
Mental Retardation, Autosomal Recessive 41
Mental Retardation, Autosomal Recessive 42
Mental Retardation, Autosomal Recessive 43
Mental Retardation, Autosomal Recessive 44
Mental Retardation, Autosomal Recessive 45
Mental Retardation, Autosomal Recessive 46
Mental Retardation, Autosomal Recessive 47
Mental Retardation, Autosomal Recessive 48
Mental Retardation, Autosomal Recessive 49
Mental Retardation, Autosomal Recessive 5
Mental Retardation, Autosomal Recessive 50
Mental Retardation, Autosomal Recessive 51
Mental Retardation, Autosomal Recessive 52
Mental Retardation, Autosomal Recessive 53
Mental Retardation, Autosomal Recessive 54
Mental Retardation, Autosomal Recessive 55
Mental Retardation, Autosomal Recessive 56
Mental Retardation, Autosomal Recessive 57
Mental Retardation, Autosomal Recessive 58
Mental Retardation, Autosomal Recessive 59
Mental Retardation, Autosomal Recessive 60
Mental Retardation, Autosomal Recessive 61
Mental Retardation Syndrome, Mietens-Weber Type
Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome
Mental Retardation with Optic Atrophy, Deafness, and Seizures
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature
Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 17
Mental Retardation, X-Linked, Syndromic 32
Mental Retardation, X-Linked, Syndromic 33
Mental Retardation, X-Linked, Syndromic 34
Mental Retardation, X-Linked, Syndromic, 35
Mental Retardation, X-Linked, Syndromic 9
Mental Retardation, X-Linked, Syndromic, Wu Type
Metachromatic Leukodystrophy
Metachromatic Leukodystrophy, Adult Form
Metachromatic Leukodystrophy, Juvenile Form
Metachromatic Leukodystrophy, Late Infantile Form
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy
Methylmalonic Aciduria and Homocystinuria, Cblc Type
Mevalonic Aciduria
Microcephaly and Chorioretinopathy 1
Microcephaly and Chorioretinopathy 2
Microcephaly and Chorioretinopathy 3
Microcephaly and Chorioretinopathy, Autosomal Recessive, 1
Microcephaly and Chorioretinopathy, Autosomal Recessive, 2
Microcephaly and Chorioretinopathy, Autosomal Recessive, 3
Microcephaly Chorioretinopathy Recessive Form
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis
Microcephaly Microcornea Syndrome Seemanova Type
Microcephaly with Chorioretinopathy, Autosomal Dominant Form
Microcoria, Congenital
Microcornea Corectopia Macular Hypoplasia
Microcornea, Glaucoma, and Absent Frontal Sinuses
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus
Microcornea Posterior Megalolenticonus Persistent Fetal Vasculature Coloboma
Microphthalmia
Microphthalmia/coloboma and Skeletal Dysplasia Syndrome
Microphthalmia, Isolated 1
Microphthalmia, Isolated 2
Microphthalmia, Isolated 3
Microphthalmia, Isolated 4
Microphthalmia, Isolated 5
Microphthalmia, Isolated 6
Microphthalmia, Isolated 7
Microphthalmia, Isolated 8
Microphthalmia, Isolated, with Cataract 1
Microphthalmia, Syndromic 1
Microphthalmia, Syndromic 10
Microphthalmia, Syndromic 11
Microphthalmia, Syndromic 12
Microphthalmia, Syndromic 13
Microphthalmia, Syndromic 2
Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 4
Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 6
Microphthalmia, Syndromic 8
Microphthalmia, Syndromic 9
Microspherophakia and/or Megalocornea, with Ectopia Lentis and with or Without Secondary Glaucoma
Microspherophakia-Metaphyseal Dysplasia
Microtia with Nasolacrimal Duct Imperforation and Eye Coloboma
Microvascular Complications of Diabetes 1
Microvascular Complications of Diabetes 2
Microvascular Complications of Diabetes 3
Microvascular Complications of Diabetes 4
Microvascular Complications of Diabetes 5
Microvascular Complications of Diabetes 6
Microvascular Complications of Diabetes 7
Mikulicz Disease
Minimal Pigment Oculocutaneous Albinism Type 1
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Mitochondrial Neurogastrointestinal Encephalomyopathy
Moebius Syndrome
Moloney Syndrome
Molybdenum Cofactor Deficiency, Complementation Group a
Molybdenum Cofactor Deficiency, Complementation Group B
Molybdenum Cofactor Deficiency, Complementation Group C
Monocular Esotropia
Monocular Exotropia
Monofixation Syndrome
Monosomy 13q34
Monosomy 21
Monosomy 22
Monosomy 9q22.3
Mooren's Ulcer
Morgagni Cataract
Mosaic Monosomy X
Mucolipidosis Ii Alpha/beta
Mucolipidosis Iii Alpha/beta
Mucolipidosis Iii Gamma
Mucolipidosis Iv
Mucopolysaccharidosis Iii
Mucopolysaccharidosis Iv
Mucopolysaccharidosis-Plus Syndrome
Mucopolysaccharidosis Type 2, Attenuated Form
Mucopolysaccharidosis Type 2, Severe Form
Mucopolysaccharidosis Type 6, Rapidly Progressing
Mucopolysaccharidosis Type 6, Slowly Progressing
Mucopolysaccharidosis, Type Ii
Mucopolysaccharidosis, Type Iiia
Mucopolysaccharidosis, Type Iiib
Mucopolysaccharidosis, Type Iiic
Mucopolysaccharidosis, Type Iiid
Mucopolysaccharidosis, Type Iva
Mucopolysaccharidosis, Type Ivb
Mucopolysaccharidosis, Type Ix
Mucopolysaccharidosis Type Vi
Mucopolysaccharidosis, Type Vii
Muir-Torre Syndrome
Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus
Multiple Familial Trichoepithelioma
Multiple Mitochondrial Dysfunctions Syndrome
Multiple Mitochondrial Dysfunctions Syndrome 1
Multiple Mitochondrial Dysfunctions Syndrome 2
Multiple Mitochondrial Dysfunctions Syndrome 3
Multiple Mitochondrial Dysfunctions Syndrome 4
Multiple Mitochondrial Dysfunctions Syndrome 5
Multiple Pterygium Syndrome, Escobar Variant
Multiple Self-Healing Squamous Epithelioma
Muscle Eye Brain Disease
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Muscular Dystrophy, Duchenne Type
Muscular Dystrophy-Dystroglycanopathy
Muscular Dystrophy-Dystroglycanopathy , Type a, 1
Muscular Dystrophy-Dystroglycanopathy , Type a, 10
Muscular Dystrophy-Dystroglycanopathy , Type a, 11
Muscular Dystrophy-Dystroglycanopathy , Type a, 12
Muscular Dystrophy-Dystroglycanopathy , Type a, 13
Muscular Dystrophy-Dystroglycanopathy , Type a, 14
Muscular Dystrophy-Dystroglycanopathy , Type a, 2
Muscular Dystrophy-Dystroglycanopathy , Type a, 3
Muscular Dystrophy-Dystroglycanopathy , Type a, 4
Muscular Dystrophy-Dystroglycanopathy , Type a, 5
Muscular Dystrophy-Dystroglycanopathy , Type a, 6
Muscular Dystrophy-Dystroglycanopathy , Type a, 7
Muscular Dystrophy-Dystroglycanopathy , Type a, 8
Muscular Dystrophy-Dystroglycanopathy , Type a, 9
Muscular Dystrophy-Dystroglycanopathy , Type B, 1
Muscular Dystrophy-Dystroglycanopathy , Type B, 14
Muscular Dystrophy-Dystroglycanopathy , Type B, 2
Muscular Dystrophy-Dystroglycanopathy , Type B, 3
Muscular Dystrophy-Dystroglycanopathy , Type B, 4
Muscular Dystrophy-Dystroglycanopathy , Type B, 5
Muscular Dystrophy-Dystroglycanopathy , Type B, 6
Muscular Dystrophy-Dystroglycanopathy , Type C, 1
Muscular Dystrophy-Dystroglycanopathy , Type C, 12
Muscular Dystrophy-Dystroglycanopathy , Type C, 14
Muscular Dystrophy-Dystroglycanopathy , Type C, 2
Muscular Dystrophy-Dystroglycanopathy , Type C, 3
Muscular Dystrophy-Dystroglycanopathy , Type C, 4
Muscular Dystrophy-Dystroglycanopathy , Type C, 5
Muscular Dystrophy-Dystroglycanopathy , Type C, 7
Muscular Dystrophy-Dystroglycanopathy , Type C, 9
Myasthenic Syndrome, Congenital, 10
Myasthenic Syndrome, Congenital, 12
Myasthenic Syndrome, Congenital, 13
Myasthenic Syndrome, Congenital, 14
Myasthenic Syndrome, Congenital, 15
Myasthenic Syndrome, Congenital, 16
Myasthenic Syndrome, Congenital, 17
Myasthenic Syndrome, Congenital, 18
Myasthenic Syndrome, Congenital, 19
Myasthenic Syndrome, Congenital, 20, Presynaptic
Myasthenic Syndrome, Congenital, 21, Presynaptic
Myasthenic Syndrome, Congenital, 22
Myasthenic Syndrome, Congenital, 5
Myasthenic Syndrome, Congenital, 6, Presynaptic
Myasthenic Syndrome, Congenital, 7, Presynaptic
Myasthenic Syndrome, Congenital, 8
Mycotic Corneal Ulcer
Myelinated Optic Nerve Fibers
Myoclonic Epilepsy Associated with Ragged-Red Fibers
Myopathy, Centronuclear, X-Linked
Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay
Myopathy, Proximal, and Ophthalmoplegia
Myopia
Myopia 10
Myopia 11, Autosomal Dominant
Myopia 12, Autosomal Dominant
Myopia 14
Myopia 15, Autosomal Dominant
Myopia 16, Autosomal Dominant
Myopia 17, Autosomal Dominant
Myopia 18, Autosomal Recessive
Myopia 19, Autosomal Dominant
Myopia 20, Autosomal Dominant
Myopia 21, Autosomal Dominant
Myopia 22, Autosomal Dominant
Myopia 23, Autosomal Recessive
Myopia 24, Autosomal Dominant
Myopia 25, Autosomal Dominant
Myopia 2, Autosomal Dominant
Myopia 3, Autosomal Dominant
Myopia 5, Autosomal Dominant
Myopia 6
Myopia 7
Myopia 8
Myopia 9
Myopic Macular Degeneration
Myotonic Cataract
Myotonic Dystrophy
Myotonic Dystrophy 1
Myotonic Dystrophy 2
Naegeli-Franceschetti-Jadassohn Syndrome
Nail-Patella Syndrome
Nance-Horan Syndrome
Nasolacrimal Duct Cyst
Nasopalpebral Lipoma-Coloboma Syndrome
Nathalie Syndrome
Neonatal Adrenoleukodystrophy
Neovascular Glaucoma
Nerve Fibre Bundle Defect
Netherton Syndrome
Neuraminidase Deficiency
Neurodegeneration with Brain Iron Accumulation
Neurodegeneration with Brain Iron Accumulation 1
Neurodegeneration with Brain Iron Accumulation 2a
Neurodegeneration with Brain Iron Accumulation 2b
Neurodegeneration with Brain Iron Accumulation 3
Neurodegeneration with Brain Iron Accumulation 4
Neurodegeneration with Brain Iron Accumulation 5
Neurodegeneration with Brain Iron Accumulation 6
Neurofibromatosis, Type I
Neurofibromatosis, Type Ii
Neurogenic Palpebral Tumor
Neuromyelitis Optica
Neuromyelitis Optica Spectrum Disorder
Neuropathy, Ataxia, and Retinitis Pigmentosa
Neuropathy, Hereditary Motor and Sensory, Type Via
Neuropathy, Hereditary Motor and Sensory, Type Vib
Neuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance
Neuropathy, Hereditary Sensory and Autonomic, Type Ia
Neuropathy, Hereditary Sensory and Autonomic, Type Ic
Neuropathy, Hereditary Sensory and Autonomic, Type Iia
Neuropathy, Hereditary Sensory and Autonomic, Type Iib
Neuropathy, Hereditary Sensory and Autonomic, Type Iii
Neuropathy, Hereditary Sensory and Autonomic, Type V
Neuropathy, Hereditary Sensory and Autonomic, Type Vi
Neuropathy, Hereditary Sensory and Autonomic, Type Vii
Neuropathy, Hereditary Sensory and Autonomic, Type Viii
Neuroretinitis
Neurotrophic Keratoconjunctivitis
Neurotrophic Keratopathy
Nevus, Epidermal
Newfoundland Rod-Cone Dystrophy
Niemann-Pick Disease
Niemann-Pick Disease, Type a
Niemann-Pick Disease, Type B
Niemann-Pick Disease, Type C1
Niemann-Pick Disease, Type C2
Niemann-Pick Disease Type C, Adult Neurologic Onset
Niemann-Pick Disease Type C, Juvenile Neurologic Onset
Niemann-Pick Disease Type C, Late Infantile Neurologic Onset
Niemann-Pick Disease Type C, Severe Early Infantile Neurologic Onset
Niemann-Pick Disease Type C, Severe Perinatal Form
Night Blindness
Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 2
Night Blindness, Congenital Stationary, Autosomal Dominant 3
Night Blindness, Congenital Stationary, Type 1a
Night Blindness, Congenital Stationary, Type 1b
Night Blindness, Congenital Stationary, Type 1c
Night Blindness, Congenital Stationary, Type 1d
Night Blindness, Congenital Stationary, Type 1e
Night Blindness, Congenital Stationary, Type 1f
Night Blindness, Congenital Stationary, Type 1g
Night Blindness, Congenital Stationary, Type 1h
Night Blindness, Congenital Stationary, Type 2a
Noble Bass Sherman Syndrome
Nodular Degeneration of Cornea
Nodular Episcleritis
Nonarteritic Anterior Ischemic Optic Neuropathy
Non-Distal Trisomy 10q
Non-Hereditary Retinoblastoma
Noninfectious Dermatoses of Eyelid
Nonsyndromic Retinitis Pigmentosa
Noonan Syndrome 1
Noonan Syndrome 10
Noonan Syndrome 2
Noonan Syndrome 3
Noonan Syndrome 4
Noonan Syndrome 5
Noonan Syndrome 6
Noonan Syndrome 7
Noonan Syndrome 8
Noonan Syndrome 9
Noonan Syndrome with Multiple Lentigines
Norrie Disease
Nuclear Senile Cataract
Nutritional Optic Neuropathy
Occult Macular Dystrophy
Ocular Albinism
Ocular Cancer
Ocular Hyperemia
Ocular Hypertension
Ocular Hypotension
Ocular Motility Disease
Ocular Motor Apraxia
Oculoauricular Syndrome
Oculo-Cerebral Dysplasia
Oculocerebral Syndrome with Hypopigmentation
Oculocutaneous Albinism
Oculodentodigital Dysplasia
Oculodentodigital Dysplasia, Autosomal Recessive
Oculodentodigital Dysplasia Dominant
Oculopharyngeal Muscular Dystrophy
Oculopharyngodistal Myopathy
Oculotrichodysplasia
Oguchi Disease 1
Oguchi Disease 2
Okihiro Syndrome Due to 20q13 Microdeletion
Okihiro Syndrome Due to a Point Mutation
Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis with Anti-Nuclear Antibodies
Oligoarticular Juvenile Idiopathic Arthritis Without Anti-Nuclear Antibodies
Oligocone Trichromacy
Oliver-Mcfarlane Syndrome
Open-Angle Glaucoma
Ophthalmia Neonatorum
Ophthalmia Nodosa
Ophthalmomandibulomelic Dysplasia
Opitz-Gbbb Syndrome
Opitz Gbbb Syndrome, Type I
Opitz Gbbb Syndrome, Type Ii
Opsoclonus-Myoclonus Syndrome
Optic Atrophy 1
Optic Atrophy 10 with or Without Ataxia, Mental Retardation, and Seizures
Optic Atrophy 11
Optic Atrophy 1 and Deafness
Optic Atrophy 2
Optic Atrophy 3, Autosomal Dominant
Optic Atrophy 4
Optic Atrophy 5
Optic Atrophy 6
Optic Atrophy 7 with or Without Auditory Neuropathy
Optic Atrophy 8
Optic Atrophy 9
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive
Optic Atrophy Opthalmoplegia Ptosis Deafness Myopia
Optic Atrophy-Peripheral Neuropathy-Developmental Delay Syndrome
Optic Atrophy--Spastic Paraplegia Syndrome
Optic Atrophy with Demyelinating Disease of Cns
Optic Atrophy with Negative Electroretinograms
Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy
Optic Disc Anomalies with Retinal and/or Macular Dystrophy
Optic Disk Drusen
Optic Nerve Astrocytoma
Optic Nerve Disease
Optic Nerve Glioma
Optic Nerve Hypoplasia, Bilateral
Optic Nerve Hypoplasia, Familial Bilateral
Optic Nerve Neoplasm
Optic Nerve Sheath Meningioma
Optic Neuritis
Opticocochleodentate Degeneration
Optic Papillitis
Optic Pathway Glioma
Optic Perineuritis
Orbital Cellulitis
Orbital Cyst
Orbital Disease
Orbital Granuloma
Orbital Leiomyoma
Orbital Margin, Hypoplasia of
Orbital Osteomyelitis
Orbital Periostitis
Orbital Plasma Cell Granuloma
Orbital Tenonitis
Orofaciodigital Syndrome
Orofaciodigital Syndrome 12
Orofaciodigital Syndrome 13
Orofaciodigital Syndrome I
Orofaciodigital Syndrome Iii
Orofaciodigital Syndrome Iv
Orofaciodigital Syndrome Ix
Orofaciodigital Syndrome V
Orofaciodigital Syndrome Vi
Orofaciodigital Syndrome Vii
Orofaciodigital Syndrome Viii
Orofaciodigital Syndrome X
Orofaciodigital Syndrome Xi
Orofaciodigital Syndrome Xiv
Orofaciodigital Syndrome Xv
Orofaciodigital Syndrome Xvi
Osteochondrodysplatic Nanism-Deafness-Retinitis Pigmentosa Syndrome
Osteopetrosis
Osteopetrosis, Autosomal Dominant 1
Osteopetrosis, Autosomal Dominant 2
Osteopetrosis, Autosomal Recessive 1
Osteopetrosis, Autosomal Recessive 2
Osteopetrosis, Autosomal Recessive 3
Osteopetrosis, Autosomal Recessive 4
Osteopetrosis, Autosomal Recessive 5
Osteopetrosis, Autosomal Recessive 6
Osteopetrosis, Autosomal Recessive 7
Osteopetrosis, Autosomal Recessive 8
Osteoporosis-Pseudoglioma Syndrome
Pagon Stephan Syndrome
Palmoplantar Carcinoma, Multiple Self-Healing
Panophthalmitis
Panuveitis
Papillary Conjunctivitis
Papilledema
Papillorenal Syndrome
Paralytic Lagophthalmos
Paralytic Squint
Paraneoplastic Uveitis
Parasitic Conjunctivitis
Parasitic Eyelid Infestation
Parkinson-Dementia Syndrome
Pars Planitis
Partial Central Choroid Dystrophy
Partial Circumpapillary Choroid Dystrophy
Partial Cryptophthalmia
Partial Optic Atrophy
Partial Third-Nerve Palsy
Patau Syndrome
Patterned Macular Dystrophy
Peho-Like Syndrome
Peho Syndrome
Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease, Classic Form
Pelizaeus-Merzbacher Disease in Female Carriers
Pelizaeus-Merzbacher Disease, Transitional Form
Pelizaeus-Merzbacher-Like Disease
Pellucid Marginal Degeneration
Perforated Corneal Ulcer
Peripheral Degeneration of Cornea
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
Peripheral Focal Chorioretinitis
Peripheral Retinal Degeneration
Peripheral Scars of Retina
Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder
Peroxisome Biogenesis Disorder 10a
Peroxisome Biogenesis Disorder 10b
Peroxisome Biogenesis Disorder 11a
Peroxisome Biogenesis Disorder 11b
Peroxisome Biogenesis Disorder 12a
Peroxisome Biogenesis Disorder 13a
Peroxisome Biogenesis Disorder 14b
Peroxisome Biogenesis Disorder 1a
Peroxisome Biogenesis Disorder 1b
Peroxisome Biogenesis Disorder 2a
Peroxisome Biogenesis Disorder 2b
Peroxisome Biogenesis Disorder 3a
Peroxisome Biogenesis Disorder 3b
Peroxisome Biogenesis Disorder 4a
Peroxisome Biogenesis Disorder 4b
Peroxisome Biogenesis Disorder 5a
Peroxisome Biogenesis Disorder 5b
Peroxisome Biogenesis Disorder 6a
Peroxisome Biogenesis Disorder 6b
Peroxisome Biogenesis Disorder 7a
Peroxisome Biogenesis Disorder 7b
Peroxisome Biogenesis Disorder 8a
Peroxisome Biogenesis Disorder 8b
Peroxisome Biogenesis Disorder 9b
Persistent Hyperplastic Primary Vitreous
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
Persistent Placoid Maculopathy
Peters Anomaly-Cataract Syndrome
Peters-Plus Syndrome
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
Phacoanaphylactic Uveitis
Phacogenic Glaucoma
Phacolytic Glaucoma
Phacomatosis Pigmentovascularis
Phakomatosis Cesioflammea
Phakomatosis Cesiomarmorata
Phakomatosis Spilorosea
Phlegmonous Dacryocystitis
Phlyctenulosis
Photokeratitis
Phthisical Cornea
Piebald Trait
Pierre Robin Syndrome
Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked
Pigmented Paravenous Chorioretinal Atrophy
Pinguecula
Plasminogen Deficiency, Type I
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract
Pontocerebellar Hypoplasia
Pontocerebellar Hypoplasia Type 1
Pontocerebellar Hypoplasia, Type 10
Pontocerebellar Hypoplasia, Type 11
Pontocerebellar Hypoplasia, Type 1a
Pontocerebellar Hypoplasia, Type 1b
Pontocerebellar Hypoplasia, Type 1c
Pontocerebellar Hypoplasia, Type 2a
Pontocerebellar Hypoplasia, Type 2b
Pontocerebellar Hypoplasia, Type 2c
Pontocerebellar Hypoplasia, Type 2d
Pontocerebellar Hypoplasia, Type 2e
Pontocerebellar Hypoplasia, Type 2f
Pontocerebellar Hypoplasia, Type 3
Pontocerebellar Hypoplasia, Type 4
Pontocerebellar Hypoplasia, Type 5
Pontocerebellar Hypoplasia, Type 6
Pontocerebellar Hypoplasia, Type 7
Pontocerebellar Hypoplasia, Type 8
Pontocerebellar Hypoplasia, Type 9
Popliteal Pterygium Syndrome
Poretti-Boltshauser Syndrome
Porphyria Cutanea Tarda
Porphyria Cutanea Tarda, Type I
Postaxial Acrofacial Dysostosis
Posterior Corneal Pigmentation
Posterior Dislocation of Lens
Posterior Polar Cataract
Posterior Scleritis
Posterior Uveal Melanoma
Posterior Uveitis
Postsynaptic Congenital Myasthenic Syndromes
Pre-Descemet Corneal Dystrophy
Preretinal Fibrosis
Presbyopia
Presynaptic Congenital Myasthenic Syndromes
Primary Angle-Closure Glaucoma
Primary Congenital Glaucoma
Primary Eye Hypotony
Primary Lacrimal Atrophy
Primary Oculocerebral Lymphoma
Primary Optic Atrophy
Progeroid Syndrome, Neonatal
Progressive Peripheral Pterygium
Progressive Supranuclear Palsy-Corticobasal Syndrome
Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome
Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome
Prolapse of Lacrimal Gland
Prolonged Electroretinal Response Suppression
Pseudo-Gaucher Disease
Pseudohypoparathyroidism
Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ib
Pseudohypoparathyroidism, Type Ic
Pseudohypoparathyroidism, Type Ii
Pseudomembranous Conjunctivitis
Pseudopapilledema
Pseudopapilledema, Ocular Hypotelorism, Blepharophimosis, and Hand Anomalies
Pseudopseudohypoparathyroidism
Pseudopterygium
Pseudoretinitis Pigmentosa
Pseudo-Turner Syndrome
Pseudoxanthoma Elasticum
Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa
Pterygium of Conjunctiva and Cornea
Ptosis
Ptosis, Hereditary Congenital 1
Ptosis, Hereditary Congenital 2
Ptosis, Strabismus, and Ectopic Pupils
Ptosis-Upper Ocular Movement Limitation-Absence of Lacrimal Punctum Syndrome
Pulsating Exophthalmos
Punctate Epithelial Keratoconjunctivitis
Pupil Disease
Purulent Endophthalmitis
Rare Isolated Myopia
Recessive Dystrophic Epidermolysis Bullosa-Generalized Other
Recurrent Corneal Erosion
Red-Green Color Blindness
Refractive Error
Refsum Disease, Classic
Regular Astigmatism
Residual Stage Angle-Closure Glaucoma
Residual Stage Corticosteroid-Induced Glaucoma
Residual Stage of Open Angle Glaucoma
Reticular Dystrophy of Retinal Pigment Epithelium
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis
Retinal Artery Occlusion
Retinal Cancer
Retinal Capillary Malformation
Retinal Cone Dystrophy 3b
Retinal Degeneration
Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma
Retinal Detachment
Retinal Disease
Retinal Drusen
Retinal Dysplasia, Primary
Retinal Dystrophies Primarily Involving Bruch's Membrane
Retinal Dystrophy and Iris Coloboma with or Without Congenital Cataract
Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome
Retinal Dystrophy with Inner Retinal Dysfunction and Ganglion Cell Abnormalities
Retinal Ischemia
Retinal Lattice Degeneration
Retinal Melanoma
Retinal Microaneurysm
Retinal Perforation
Retinal Telangiectasia
Retinal Vascular Disease
Retinal Vascular Occlusion
Retinal Vasculitis
Retina Lymphoma
Retinitis
Retinitis Pigmentosa
Retinitis Pigmentosa 1
Retinitis Pigmentosa 10
Retinitis Pigmentosa 11
Retinitis Pigmentosa 12
Retinitis Pigmentosa 13
Retinitis Pigmentosa 14
Retinitis Pigmentosa 17
Retinitis Pigmentosa 18
Retinitis Pigmentosa 19
Retinitis Pigmentosa 2
Retinitis Pigmentosa 20
Retinitis Pigmentosa 22
Retinitis Pigmentosa 23
Retinitis Pigmentosa 24
Retinitis Pigmentosa 25
Retinitis Pigmentosa 26
Retinitis Pigmentosa 27
Retinitis Pigmentosa 28
Retinitis Pigmentosa 29
Retinitis Pigmentosa 2, X-Linked
Retinitis Pigmentosa 3
Retinitis Pigmentosa 30
Retinitis Pigmentosa 31
Retinitis Pigmentosa 32
Retinitis Pigmentosa 33
Retinitis Pigmentosa 34
Retinitis Pigmentosa 35
Retinitis Pigmentosa 36
Retinitis Pigmentosa 37
Retinitis Pigmentosa 38
Retinitis Pigmentosa 39
Retinitis Pigmentosa 4
Retinitis Pigmentosa 40
Retinitis Pigmentosa 41
Retinitis Pigmentosa 42
Retinitis Pigmentosa 43
Retinitis Pigmentosa 44
Retinitis Pigmentosa 45
Retinitis Pigmentosa 46
Retinitis Pigmentosa 47
Retinitis Pigmentosa 48
Retinitis Pigmentosa 49
Retinitis Pigmentosa 50
Retinitis Pigmentosa 51
Retinitis Pigmentosa 54
Retinitis Pigmentosa 55
Retinitis Pigmentosa 56
Retinitis Pigmentosa 57
Retinitis Pigmentosa 58
Retinitis Pigmentosa 59
Retinitis Pigmentosa 6
Retinitis Pigmentosa 60
Retinitis Pigmentosa 61
Retinitis Pigmentosa 62
Retinitis Pigmentosa 63
Retinitis Pigmentosa 66
Retinitis Pigmentosa 67
Retinitis Pigmentosa 68
Retinitis Pigmentosa 69
Retinitis Pigmentosa 7
Retinitis Pigmentosa 70
Retinitis Pigmentosa 71
Retinitis Pigmentosa 72
Retinitis Pigmentosa 73
Retinitis Pigmentosa 74
Retinitis Pigmentosa 75
Retinitis Pigmentosa 76
Retinitis Pigmentosa 77
Retinitis Pigmentosa 78
Retinitis Pigmentosa 79
Retinitis Pigmentosa 80
Retinitis Pigmentosa 81
Retinitis Pigmentosa 9
Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism
Retinitis Pigmentosa, Late-Adult Onset
Retinitis Pigmentosa with or Without Situs Inversus
Retinitis Pigmentosa, X-Linked, and Sinorespiratory Infections, with or Without Deafness
Retinitis Pigmentosa, Y-Linked
Retinoblastoma
Retinochoroidal Coloboma
Retinopathy, Arteriosclerotic
Retinopathy, Pericentral Pigmentary, Autosomal Recessive
Retinopathy, Pericentral Pigmentary, Dominant
Retinoschisis 1, X-Linked, Juvenile
Revesz Syndrome
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis with Anti-Nuclear Antibodies
Rheumatoid Factor-Negative Juvenile Idiopathic Arthritis Without Anti-Nuclear Antibodies
Rhizomelic Chondrodysplasia Punctata
Rhizomelic Chondrodysplasia Punctata, Type 1
Rhizomelic Chondrodysplasia Punctata, Type 2
Rhizomelic Chondrodysplasia Punctata, Type 3
Rhizomelic Chondrodysplasia Punctata, Type 5
Rhyns Syndrome
Ring Corneal Ulcer
Ring Dermoid of Cornea
Ring Staphyloma
Roberts Syndrome
Rodrigues Blindness
Rosacea Conjunctivitis
Rothmund-Thomson Syndrome
Rothmund-Thomson Syndrome Type 1
Rothmund-Thomson Syndrome Type 2
Rubeosis Iridis
Rubinstein Taybi Like Syndrome
Rubinstein-Taybi Syndrome 1
Rubinstein-Taybi Syndrome 2
Rutherfurd Syndrome
Saethre-Chotzen Syndrome
Sandhoff Disease
Sarcoidosis 1
Sarcoidosis 2
Sarcoidosis 3
Scheie Syndrome
Schimmelpenning-Feuerstein-Mims Syndrome
Schnyder Corneal Dystrophy
Schopf-Schulz-Passarge Syndrome
Schwartz-Jampel Syndrome, Type 1
Scleral Disease
Scleral Staphyloma
Scleritis
Sclerocornea
Sclerocornea, Autosomal Dominant
Scleromalacia Perforans
Scleroperikeratitis
Sclerosing Keratitis
Scoliosis, Arachnodactyly, and Blindness
Scotoma
Secondary Corneal Edema
Secondary Lacrimal Atrophy
Secondary Vitreoretinal Degeneration
Seizures, Cortical Blindness, and Microcephaly Syndrome
Senile Atrophy of Choroid
Senile Cataract
Senile Ectropion
Senile Entropion
Senile Reticular Retinal Degeneration
Senior-Loken Syndrome 1
Senior-Loken Syndrome 3
Senior-Loken Syndrome 4
Senior-Loken Syndrome 5
Senior-Loken Syndrome 6
Senior-Loken Syndrome 7
Senior-Loken Syndrome 8
Senior-Loken Syndrome 9
Septooptic Dysplasia
Septo-Optic Dysplasia Spectrum
Serous Conjunctivitis Except Viral
Serpiginous Choroiditis
Severe Early-Childhood-Onset Retinal Dystrophy
Severe Intellectual Disability-Hypotonia-Strabismus-Coarse Face-Planovalgus Syndrome
Severe Nonproliferative Diabetic Retinopathy
Shipyard Eye
Short Qt Syndrome
Short Qt Syndrome 1
Short Qt Syndrome 2
Short Qt Syndrome 3
Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly
Short Stature, Hearing Loss, Retinitis Pigmentosa, and Distinctive Facies
Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly
Short Stature with Optic Atrophy and Pelger-Huët Anomaly Syndrome
Short Syndrome
Short Tarsus with Absence of Lower Eyelashes
Siderosis
Siderosis of Eye
Silengo Lerone Pelizza Syndrome
Simple Chronic Conjunctivitis
Sjogren-Larsson-Like Syndrome
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Solar Retinopathy
Sorsby Fundus Dystrophy
Sotos Syndrome 1
Sotos Syndrome 2
Sotos Syndrome 3
Spasmus Nutans
Spastic Ataxia
Spastic Ataxia 1
Spastic Ataxia 1, Autosomal Dominant
Spastic Ataxia 2
Spastic Ataxia 2, Autosomal Recessive
Spastic Ataxia 3
Spastic Ataxia 3, Autosomal Recessive
Spastic Ataxia 4
Spastic Ataxia 4, Autosomal Recessive
Spastic Ataxia 5
Spastic Ataxia 5, Autosomal Recessive
Spastic Ataxia 7
Spastic Ataxia 7, Autosomal Dominant
Spastic Ectropion
Spastic Entropion
Spastic Paraplegia 1
Spastic Paraplegia 10
Spastic Paraplegia 10, Autosomal Dominant
Spastic Paraplegia 11
Spastic Paraplegia 11, Autosomal Recessive
Spastic Paraplegia 12
Spastic Paraplegia 12, Autosomal Dominant
Spastic Paraplegia 13
Spastic Paraplegia 13, Autosomal Dominant
Spastic Paraplegia 14
Spastic Paraplegia 14, Autosomal Recessive
Spastic Paraplegia 15
Spastic Paraplegia 15, Autosomal Recessive
Spastic Paraplegia 16
Spastic Paraplegia 16, X-Linked
Spastic Paraplegia 17
Spastic Paraplegia 17, Autosomal Dominant
Spastic Paraplegia 18
Spastic Paraplegia 18, Autosomal Recessive
Spastic Paraplegia 19
Spastic Paraplegia 19, Autosomal Dominant
Spastic Paraplegia 20, Autosomal Recessive
Spastic Paraplegia 23
Spastic Paraplegia 24
Spastic Paraplegia 24, Autosomal Recessive
Spastic Paraplegia 25
Spastic Paraplegia 25, Autosomal Recessive
Spastic Paraplegia 26
Spastic Paraplegia 26, Autosomal Recessive
Spastic Paraplegia 27, Autosomal Recessive
Spastic Paraplegia 28, Autosomal Recessive
Spastic Paraplegia 29
Spastic Paraplegia 29, Autosomal Dominant
Spastic Paraplegia 2, X-Linked
Spastic Paraplegia 3
Spastic Paraplegia 30, Autosomal Recessive
Spastic Paraplegia 31
Spastic Paraplegia 31, Autosomal Dominant
Spastic Paraplegia 32
Spastic Paraplegia 32, Autosomal Recessive
Spastic Paraplegia 33, Autosomal Dominant
Spastic Paraplegia 34, X-Linked
Spastic Paraplegia 35, Autosomal Recessive
Spastic Paraplegia 36, Autosomal Dominant
Spastic Paraplegia 37, Autosomal Dominant
Spastic Paraplegia 38, Autosomal Dominant
Spastic Paraplegia 39
Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 3a
Spastic Paraplegia 3, Autosomal Dominant
Spastic Paraplegia 4
Spastic Paraplegia 41, Autosomal Dominant
Spastic Paraplegia 42, Autosomal Dominant
Spastic Paraplegia 43, Autosomal Recessive
Spastic Paraplegia 44, Autosomal Recessive
Spastic Paraplegia 45, Autosomal Recessive
Spastic Paraplegia 46, Autosomal Recessive
Spastic Paraplegia 47, Autosomal Recessive
Spastic Paraplegia 48, Autosomal Recessive
Spastic Paraplegia 49, Autosomal Recessive
Spastic Paraplegia 4, Autosomal Dominant
Spastic Paraplegia 50, Autosomal Recessive
Spastic Paraplegia 51
Spastic Paraplegia 51, Autosomal Recessive
Spastic Paraplegia 52, Autosomal Recessive
Spastic Paraplegia 53, Autosomal Recessive
Spastic Paraplegia 54, Autosomal Recessive
Spastic Paraplegia 55, Autosomal Recessive
Spastic Paraplegia 56, Autosomal Recessive
Spastic Paraplegia 57, Autosomal Recessive
Spastic Paraplegia 5a
Spastic Paraplegia 5a, Autosomal Recessive
Spastic Paraplegia 5b
Spastic Paraplegia 6
Spastic Paraplegia 61, Autosomal Recessive
Spastic Paraplegia 62, Autosomal Recessive
Spastic Paraplegia 63, Autosomal Recessive
Spastic Paraplegia 64, Autosomal Recessive
Spastic Paraplegia 6, Autosomal Dominant
Spastic Paraplegia 72, Autosomal Recessive
Spastic Paraplegia 73, Autosomal Dominant
Spastic Paraplegia 74, Autosomal Recessive
Spastic Paraplegia 75, Autosomal Recessive
Spastic Paraplegia 76, Autosomal Recessive
Spastic Paraplegia 77, Autosomal Recessive
Spastic Paraplegia 78, Autosomal Recessive
Spastic Paraplegia 79, Autosomal Recessive
Spastic Paraplegia 7, Autosomal Recessive
Spastic Paraplegia 8
Spastic Paraplegia 8, Autosomal Dominant
Spastic Paraplegia 9
Spastic Paraplegia 9a, Autosomal Dominant
Spastic Paraplegia 9b, Autosomal Recessive
Spastic Paraplegia, Optic Atrophy, and Dementia
Spastic Paraplegia, Optic Atrophy, and Neuropathy
Spastic Paraplegia, Optic Atrophy, Microcephaly, and Xy Sex Reversal
Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
Spatial Visualization, Aptitude for
Spinocerebellar Ataxia 1
Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 11
Spinocerebellar Ataxia 12
Spinocerebellar Ataxia 13
Spinocerebellar Ataxia 14
Spinocerebellar Ataxia 15
Spinocerebellar Ataxia 17
Spinocerebellar Ataxia 18
Spinocerebellar Ataxia 19
Spinocerebellar Ataxia 2
Spinocerebellar Ataxia 20
Spinocerebellar Ataxia 21
Spinocerebellar Ataxia 23
Spinocerebellar Ataxia 25
Spinocerebellar Ataxia 26
Spinocerebellar Ataxia 27
Spinocerebellar Ataxia 28
Spinocerebellar Ataxia 29
Spinocerebellar Ataxia 30
Spinocerebellar Ataxia 31
Spinocerebellar Ataxia 32
Spinocerebellar Ataxia 34
Spinocerebellar Ataxia 35
Spinocerebellar Ataxia 36
Spinocerebellar Ataxia 37
Spinocerebellar Ataxia 38
Spinocerebellar Ataxia 4
Spinocerebellar Ataxia 40
Spinocerebellar Ataxia 41
Spinocerebellar Ataxia 42
Spinocerebellar Ataxia 43
Spinocerebellar Ataxia 44
Spinocerebellar Ataxia 45
Spinocerebellar Ataxia 46
Spinocerebellar Ataxia 5
Spinocerebellar Ataxia 6
Spinocerebellar Ataxia 7
Spinocerebellar Ataxia 8
Spinocerebellar Ataxia 9
Spinocerebellar Ataxia, Autosomal Recessive 1
Spinocerebellar Ataxia, Autosomal Recessive 10
Spinocerebellar Ataxia, Autosomal Recessive 11
Spinocerebellar Ataxia, Autosomal Recessive 12
Spinocerebellar Ataxia, Autosomal Recessive 13
Spinocerebellar Ataxia, Autosomal Recessive 14
Spinocerebellar Ataxia, Autosomal Recessive 15
Spinocerebellar Ataxia, Autosomal Recessive 16
Spinocerebellar Ataxia, Autosomal Recessive 17
Spinocerebellar Ataxia, Autosomal Recessive 18
Spinocerebellar Ataxia, Autosomal Recessive 2
Spinocerebellar Ataxia, Autosomal Recessive 20
Spinocerebellar Ataxia, Autosomal Recessive 21
Spinocerebellar Ataxia, Autosomal Recessive 22
Spinocerebellar Ataxia, Autosomal Recessive 23
Spinocerebellar Ataxia, Autosomal Recessive 24
Spinocerebellar Ataxia, Autosomal Recessive 25
Spinocerebellar Ataxia, Autosomal Recessive 26
Spinocerebellar Ataxia, Autosomal Recessive 3
Spinocerebellar Ataxia, Autosomal Recessive 4
Spinocerebellar Ataxia Autosomal Recessive 5
Spinocerebellar Ataxia, Autosomal Recessive 6
Spinocerebellar Ataxia, Autosomal Recessive 7
Spinocerebellar Ataxia, Autosomal Recessive 8
Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy
Spinocerebellar Ataxia Type 16
Spinocerebellar Ataxia Type 19/22
Spinocerebellar Ataxia Type 1 with Axonal Neuropathy
Spinocerebellar Ataxia with Axonal Neuropathy Type 2
Spinocerebellar Ataxia, X-Linked 1
Spinocerebellar Ataxia, X-Linked 2
Spinocerebellar Ataxia, X-Linked 3
Spinocerebellar Ataxia, X-Linked 4
Spinocerebellar Ataxia, X-Linked 5
Spinocerebellar Degeneration and Corneal Dystrophy
Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia
Splenomegaly, Cytopenia, and Vision Loss
Spondyloocular Syndrome
Spontaneous Ocular Nystagmus
Squamous Blepharitis
Stable Condition Keratoconus
Staphyloma Posticum
Stargardt Disease
Stargardt Disease 1
Stargardt Disease 3
Stargardt Disease 4
Stenosis of Lacrimal Passage
Stenosis of Lacrimal Punctum
Stenosis of Lacrimal Sac
Steroid-Induced Glaucoma
Steroid-Induced Glaucoma - Borderline
Stickler Syndrome
Stickler Syndrome, Type 3
Stickler Syndrome, Type I
Stickler Syndrome, Type Ii
Stickler Syndrome, Type I, Nonsyndromic Ocular
Stickler Syndrome, Type Iv
Stickler Syndrome, Type V
Strabismus
Stromal Corneal Pigmentation
Stromal Dystrophy
Stromal Keratitis
Sturge-Weber Syndrome
Subaortic Stenosis--Short Stature Syndrome
Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency
Sulfite Oxidase Deficiency, Isolated
Superficial Keratitis
Superior Limbic Keratoconjunctivitis
Suppression Amblyopia
Suppurative Uveitis
Supranuclear Palsy, Progressive, 1
Supranuclear Palsy, Progressive, 2
Supranuclear Palsy, Progressive, 3
Sveinsson Chorioretinal Atrophy
Sympathetic Ophthalmia
Tarsal Kink Syndrome
Tay-Sachs Disease
Tay-Sachs Disease, B1 Variant
Tay-Sachs Disease, B Variant, Adult Form
Tay-Sachs Disease, B Variant, Infantile Form
Tay-Sachs Disease, B Variant, Juvenile Form
Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, Type 2
Telangiectasia, Hereditary Hemorrhagic, Type 3
Telangiectasia, Hereditary Hemorrhagic, Type 4
Telangiectasia, Hereditary Hemorrhagic, Type 5
Tented Eyebrows
Tetanic Cataract
Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities
Tetrasomy 15q26
Tetrasomy 5p
Thyrotoxic Exophthalmos
Tietz Albinism-Deafness Syndrome
Tolosa-Hunt Syndrome
Total Circumpapillary Dystrophy of Choroid
Total Internal Ophthalmoplegia
Total Third-Nerve Palsy
Toxic Maculopathy
Toxic Maculopathy Due to Antimalarial Drugs
Toxic Optic Neuropathy
Transient Refractive Change
Traumatic Glaucoma
Treacher Collins Syndrome 1
Treacher Collins Syndrome 2
Treacher Collins Syndrome 3
Trichoepithelioma, Multiple Familial, 1
Trichoepithelioma, Multiple Familial, 2
Trichomegaly
Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina
Triploidy
Tristichiasis
Tritanopia
Tuberous Sclerosis
Tuberous Sclerosis 1
Tuberous Sclerosis 2
Tubulointerstitial Nephritis with Uveitis
Tukel Syndrome
Turner Syndrome
Turner Syndrome Due to Structural X Chromosome Anomalies
Tyrosinemia
Tyrosinemia, Type I
Tyrosinemia, Type Ii
Tyrosinemia, Type Iii
Ulcerative Blepharitis
Ulerythema Ophryogenesis
Usher Syndrome
Usher Syndrome Type 2
Usher Syndrome, Type 2b
Usher Syndrome, Type I
Usher Syndrome, Type Ic
Usher Syndrome, Type Id
Usher Syndrome, Type if
Usher Syndrome, Type Ig
Usher Syndrome, Type Ih
Usher Syndrome, Type Iia
Usher Syndrome, Type Iic
Usher Syndrome, Type Iid
Usher Syndrome, Type Iiia
Usher Syndrome, Type Iiib
Usher Syndrome, Type Ij
Usher Syndrome, Type Ik
Uveitis
Vasoproliferative Tumor of the Retina
Venous Tributary Occlusion of Retina
Vernal Conjunctivitis
Vernal Keratoconjunctivitis
Vertebral Fusion, Posterior Lumbosacral, with Blepharoptosis
Vestibular Nystagmus
Vici Syndrome
Visceral Myopathy, Familial, with External Ophthalmoplegia
Visual Agnosia
Visual Cortex Disease
Visual Epilepsy
Visual Pathway and Hypothalamic Glioma, Childhood
Visual Pathway Disease
Visual Snow Syndrome
Visual Verbal Agnosia
Vitamin E, Familial Isolated Deficiency of
Vitelliform Macular Dystrophy
Vitreoretinal Degeneration
Vitreoretinal Degeneration, Snowflake Type
Vitreoretinal Dystrophy
Vitreoretinochoroidopathy
Vitreoretinochoroidopathy Dominant
Vitreoretinopathy, Neovascular Inflammatory
Vitreous Abscess
Vitreous Detachment
Vitreous Disease
Vitreous Syneresis
Vocal Cord Paralysis and Ptosis
Vogt-Koyanagi-Harada Disease
Von Hippel-Lindau Syndrome
Waardenburg's Syndrome
Waardenburg Syndrome, Type 1
Waardenburg Syndrome, Type 2a
Waardenburg Syndrome, Type 2b
Waardenburg Syndrome, Type 2c
Waardenburg Syndrome, Type 2d
Waardenburg Syndrome, Type 2e
Waardenburg Syndrome, Type 3
Waardenburg Syndrome Type 4
Waardenburg Syndrome, Type 4a
Waardenburg Syndrome, Type 4b
Waardenburg Syndrome, Type 4c
Wagner Vitreoretinopathy
Walker-Warburg Syndrome
Warburg Micro Syndrome
Warburg Micro Syndrome 1
Warburg Micro Syndrome 2
Warburg Micro Syndrome 3
Warburg Micro Syndrome 4
Webb-Dattani Syndrome
Weill-Marchesani-Like Syndrome
Weill-Marchesani Syndrome
Weill-Marchesani Syndrome 1
Weill-Marchesani Syndrome 2
Weill-Marchesani Syndrome 3
Werner Syndrome
Williams-Beuren Syndrome
Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome
Wilson Disease
Wolfram-Like Syndrome, Autosomal Dominant
Wolfram Syndrome
Wolfram Syndrome 1
Wolfram Syndrome 2
Wolfram Syndrome, Mitochondrial Form
Wrinkly Skin Syndrome
Wyburn Mason's Syndrome
Xeroderma of Eyelid
Xerophthalmia
X-Linked Charcot-Marie-Tooth Disease
X-Linked Chondrodysplasia Punctata
X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome
X-Linked Keloid Scarring-Reduced Joint Mobility-Increased Optic Cup-to-Disc Ratio Syndrome
You-Hoover-Fong Syndrome |
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