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| Boli A-Z | | 13q12.3 Microdeletion Syndrome
46 Xx Gonadal Dysgenesis
46 Xy Gonadal Dysgenesis
9q33.3q34.11 Microdeletion Syndrome
Aarskog-Scott Syndrome
Ablepharon-Macrostomia Syndrome
Absence of Fingerprints Congenital Milia
Acantholytic Squamous Cell Skin Carcinoma
Acanthosis Nigricans
Acanthosis Nigricans with Muscle Cramps and Acral Enlargement
Achenbach Syndrome
Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans
Ackerman Syndrome
Acneiform Dermatitis
Acquired Angioedema
Acquired Angioedema Type 1
Acquired Angioedema Type 2
Acquired Cutis Laxa
Acquired Generalized Lipodystrophy
Acquired Hyperkeratosis
Acquired Kinky Hair Syndrome
Acquired Pseudoxanthoma Elasticum
Acral Dystrophic Epidermolysis Bullosa
Acral Lentiginous Melanoma
Acral Persistent Papular Mucinosis
Acral Self-Healing Collodion Baby
Acrocephalopolydactylous Dysplasia
Acrodermatitis
Acrodermatitis Chronica Atrophicans
Acrodermatitis Enteropathica, Zinc-Deficiency Type
Acrogeria, Gottron Type
Acrokeratoderma, Hereditary Papulotranslucent
Acrokeratosis Verruciformis
Acromegaloid Hypertrichosis Syndrome
Acromelanosis
Acrospiroma
Actinic Keratosis
Actinic Lichen Planus
Actinic Prurigo
Acute Generalized Exanthematous Pustulosis
Acute T Cell Leukemia
Adamantinoid Basal Cell Epithelioma
Adams-Oliver Syndrome
Adams-Oliver Syndrome 1
Adams-Oliver Syndrome 2
Adams-Oliver Syndrome 3
Adams-Oliver Syndrome 4
Adams-Oliver Syndrome 5
Adams-Oliver Syndrome 6
Adenoid Basal Cell Carcinoma
Adenosine Deaminase 2 Deficiency
Adermatoglyphia
Adiposis Dolorosa
Adrenoleukodystrophy
Adult Dermatomyositis
Adult Leptomeningeal Melanoma
Adult Syndrome
Adult T-Cell Leukemia
Adult Xanthogranuloma
Agammaglobulinemia, Microcephaly, and Severe Dermatitis
Agenesis of the Corpus Callosum with Peripheral Neuropathy
Ainhum
Albinism-Deafness Syndrome
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
Al Gazali Aziz Salem Syndrome
Alkaptonuria
Allergic Contact Dermatitis
Allergic Contact Dermatitis of Eyelid
Allergic Urticaria
Alopecia Antibody Deficiency
Alopecia Areata
Alopecia Areata 1
Alopecia Areata 2
Alopecia-Contractures-Dwarfism Mental Retardation Syndrome
Alopecia-Epilepsy-Oligophrenia Syndrome of Moynahan
Alopecia-Intellectual Disability Syndrome
Alopecia Intellectual Disability Syndrome 2
Alopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality
Alopecia Totalis
Alopecia Universalis Congenita
Amelanotic Melanoma
Ameloonychohypohidrotic Syndrome
Amyloidosis Cutis Dyschromia
Amyloidosis Nodular Localized Cutaneous
Amyloidosis, Primary Localized Cutaneous, 1
Amyloidosis, Primary Localized Cutaneous, 2
Anal Margin Basal Cell Carcinoma
Anal Margin Carcinoma
Anal Margin Squamous Cell Carcinoma
Anal Squamous Cell Carcinoma
Androgenic Alopecia
Angioedema
Angioedema, Hereditary, Type I
Angioedema, Hereditary, Type Iii
Angiokeratoma
Angiolipomatosis, Familial
Angioma Serpiginosum
Angioma Serpiginosum, Autosomal Dominant
Angiomatosis, Diffuse Corticomeningeal, of Divry and Van Bogaert
Angioma, Tufted
Angioosteohypertrophic Syndrome
Angora Hair Nevus
Anhidrosis
Anhidrosis, Isolated, with Normal Sweat Glands
Annular Atrophic Lichen Planus
Annular Lichen Planus
Anonychia with Flexural Pigmentation
Anterior Cutaneous Nerve Entrapment Syndrome
Anti-P200 Pemphigoid
Aplasia Cutis Congenita
Aplasia Cutis Congenita Dominant
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction
Aplasia Cutis Congenita, Nonsyndromic
Aplasia Cutis Congenita of Limbs, Autosomal Recessive
Aplasia Cutis Congenita of Limbs Recessive
Aplasia Cutis Congenita Recessive
Aplasia Cutis Congenita with Intestinal Lymphangiectasia
Apocrine Adenocarcinoma
Aquagenic Syringeal Acrokeratoderm
Aredyld
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
Arterial Tortuosity Syndrome
Arthrochalasia Ehlers-Danlos Syndrome
Arthrogryposis and Ectodermal Dysplasia
Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/palate, and Developmental Delay
Ataxia-Telangiectasia
Ataxia-Telangiectasia-Like Disorder 1
Ataxia-Telangiectasia-Like Disorder 2
Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death
Atp6v0a2-Related Cutis Laxa
Atrichia with Papular Lesions
Atrophia Maculosa Varioliformis Cutis, Familial
Atrophic Lichen Planus
Atrophoderma of Pierini and Pasini
Atrophoderma Vermiculata
Atypical Lichen Myxedematosus
Autoimmune Disease of Skin and Connective Tissue
Autoimmune Progesterone Dermatitis
Autoinflammation, Lipodystrophy, and Dermatosis Syndrome
Autoinflammation, Panniculitis, and Dermatosis Syndrome
Autosomal Dominant Deafness-Onychodystrophy Syndrome
Autosomal Dominant Palmoplantar Keratoderma and Congenital Alopecia
Autosomal Dominant Preaxial Polydactyly-Upperback Hypertrichosis Syndrome
Autosomal Dominant Trichoodontoonychodysplasia-Syndactyly
Autosomal Recessive Congenital Ichthyosis
Autosomal Recessive Cutis Laxa Type 2, Classic Type
Autosomal Recessive Palmoplantar Keratoderma and Congenital Alopecia
Autosomal Recessive Type Iv Ehlers-Danlos Syndrome
Autosomal Semi-Dominant Severe Lipodystrophic Laminopathy
Bacterial Exanthem
Balloon Cell Malignant Melanoma
Bannayan-Riley-Ruvalcaba Syndrome
Bap1 Tumor Predisposition Syndrome
Barber-Say Syndrome
Basal Cell Carcinoma
Basal Cell Carcinoma 1
Basal Cell Carcinoma 2
Basal Cell Carcinoma 3
Basal Cell Carcinoma 4
Basal Cell Carcinoma 5
Basal Cell Carcinoma 6
Basal Cell Carcinoma 7
Basal Cell Carcinoma, Infundibulocystic
Basal Cell Carcinoma, Multiple
Basal Cell Nevus Syndrome
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant
Basaloid Squamous Cell Skin Carcinoma
Basan Syndrome
Basaran Yilmaz Syndrome
Bazex Syndrome
Beare-Stevenson Cutis Gyrata Syndrome
Becker Nevus Syndrome
Bednar Tumor
Behcet Syndrome
Benign Cephalic Histiocytosis
Benign Chronic Pemphigus
Benign Dermal Neurilemmoma
Bier Spots
Biotinidase Deficiency
Birt-Hogg-Dube Syndrome
Bjornstad Syndrome
Bladder Squamous Cell Carcinoma
Blastomycosis
Blau Syndrome
Blepharocheilodontic Syndrome 1
Blepharocheilodontic Syndrome 2
Bloom Syndrome
Blue Rubber Bleb Nevus
Book Syndrome
Borrone Di Rocco Crovato Syndrome
Boudhina Yedes Khiari Syndrome
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism
Brittle Cornea Syndrome 1
Brittle Cornea Syndrome 2
Brooke-Spiegler Syndrome
Bullous Diffuse Cutaneous Mastocytosis
Bullous Dystrophy, Hereditary Macular Type
Bullous Impetigo
Bullous Lichen Planus
Bullous Pemphigoid
Bullous Skin Disease
Buschke-Ollendorff Syndrome
Cafe-Au-Lait Spots, Multiple
Cahmr Syndrome
Calcifying Aponeurotic Fibroma
Calciphylaxis Cutis
Callosities, Hereditary Painful
Campomelia, Cumming Type
Candidal Paronychia
Candidiasis
Candidiasis, Familial, 1
Candidiasis, Familial, 2
Candidiasis, Familial, 3
Candidiasis, Familial, 4
Candidiasis, Familial, 6
Candidiasis, Familial, 8
Candidiasis, Familial, 9
Capillary Hemangioma
Capillary Lymphangioma
Capillary Malformations, Congenital
Carbuncle
Cardiofaciocutaneous Syndrome 1
Cardiofaciocutaneous Syndrome 2
Cardiofaciocutaneous Syndrome 3
Cardiofaciocutaneous Syndrome 4
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma
Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis
Carney Complex, Type 1
Carney Complex, Type 2
Carney Complex Variant
Cdk4 Linked Melanoma
Cell Type Benign Neoplasm
Cell Type Cancer
Cellulitis
Centripetalis Recessive Dystrophic Epidermolysis Bullosa
Cercarial Dermatitis
Cerebellar Ataxia and Ectodermal Dysplasia
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 Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome
Cerebrotendinous Xanthomatosis
Ceruminous Carcinoma
Cervix Melanoma
Chanarin-Dorfman Syndrome
Chancroid
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2a2b
Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2b
Charcot-Marie-Tooth Disease, Axonal, Type 2b1
Charcot-Marie-Tooth Disease, Axonal, Type 2b2
Charcot-Marie-Tooth Disease, Axonal, Type 2cc
Charcot-Marie-Tooth Disease, Axonal, Type 2d
Charcot-Marie-Tooth Disease, Axonal, Type 2e
Charcot-Marie-Tooth Disease, Axonal, Type 2f
Charcot-Marie-Tooth Disease, Axonal, Type 2h
Charcot-Marie-Tooth Disease, Axonal, Type 2i
Charcot-Marie-Tooth Disease, Axonal, Type 2j
Charcot-Marie-Tooth Disease, Axonal, Type 2k
Charcot-Marie-Tooth Disease, Axonal, Type 2l
Charcot-Marie-Tooth Disease, Axonal, Type 2n
Charcot-Marie-Tooth Disease, Axonal, Type 2o
Charcot-Marie-Tooth Disease, Axonal, Type 2p
Charcot-Marie-Tooth Disease, Axonal, Type 2q
Charcot-Marie-Tooth Disease, Axonal, Type 2r
Charcot-Marie-Tooth Disease, Axonal, Type 2t
Charcot-Marie-Tooth Disease, Axonal, Type 2u
Charcot-Marie-Tooth Disease, Axonal, Type 2v
Charcot-Marie-Tooth Disease, Axonal, Type 2w
Charcot-Marie-Tooth Disease, Axonal, Type 2x
Charcot-Marie-Tooth Disease, Axonal, Type 2z
Chediak-Higashi Syndrome
Cheilitis Glandularis
Chilblain Lupus 1
Chilblain Lupus 2
Childhood Type Dermatomyositis
Cholestasis-Lymphedema Syndrome
Cholesteatoma
Cholesteatoma, Congenital
Cholesteatoma of Attic
Cholesteatoma of External Ear
Cholesteatoma of Middle Ear
Cholinergic Urticaria
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
Choreoacanthocytosis
Choroid Epithelioid Cell Melanoma
Choroid Mixed Cell Melanoma
Choroid Necrotic Melanoma
Choroid Spindle Cell Melanoma
Chromhidrosis
Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb
Chronic Actinic Dermatitis
Chronic Granulomatous Disease
Chronic Mucocutaneous Candidiasis
Chronic Recurrent Multifocal Osteomyelitis
Chronic Ulcer of Skin
Cicatricial Pemphigoid
Ciliary Body Epithelioid Cell Melanoma
Ciliary Body Mixed Cell Melanoma
Ciliary Body Spindle Cell Melanoma
Cinca Syndrome
Circumscribed Palmoplantar Hypokeratosis
Clear Cell Basal Cell Carcinoma
Clear Cell Hidradenoma
Clear Cell Sarcoma
Clear Cell Squamous Cell Skin Carcinoma
Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa
Clouston Syndrome
Cobb Syndrome
Cockayne Syndrome
Cockayne Syndrome a
Cockayne Syndrome B
Cockayne Syndrome Type I
Cockayne Syndrome Type Ii
Cockayne Syndrome Type Iii
Cold Urticaria
Cole Disease
Collagenoma, Familial Cutaneous
Collagenosis, Familial Reactive Perforating
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome
Colon Squamous Cell Carcinoma
Combined Cellular and Humoral Immune Defects with Granulomas
Complement Component 5 Deficiency
Complement Component 9 Deficiency
Confetti-Like Macular Atrophy
Congenital Disorder of Glycosylation, Type Ia
Congenital Disorder of Glycosylation, Type Ib
Congenital Disorder of Glycosylation, Type Ic
Congenital Disorder of Glycosylation, Type Id
Congenital Disorder of Glycosylation, Type Ie
Congenital Disorder of Glycosylation, Type if
Congenital Disorder of Glycosylation, Type Ig
Congenital Disorder of Glycosylation, Type Ih
Congenital Disorder of Glycosylation, Type Ii
Congenital Disorder of Glycosylation, Type Iia
Congenital Disorder of Glycosylation, Type Iib
Congenital Disorder of Glycosylation, Type Iic
Congenital Disorder of Glycosylation, Type Iid
Congenital Disorder of Glycosylation, Type Iif
Congenital Disorder of Glycosylation, Type Iig
Congenital Disorder of Glycosylation, Type Iih
Congenital Disorder of Glycosylation, Type Iii
Congenital Disorder of Glycosylation, Type I/iix
Congenital Disorder of Glycosylation, Type Iij
Congenital Disorder of Glycosylation, Type Iik
Congenital Disorder of Glycosylation, Type Iil
Congenital Disorder of Glycosylation, Type Iim
Congenital Disorder of Glycosylation, Type Iin
Congenital Disorder of Glycosylation, Type Iio
Congenital Disorder of Glycosylation, Type Iip
Congenital Disorder of Glycosylation, Type Iiq
Congenital Disorder of Glycosylation, Type Ij
Congenital Disorder of Glycosylation, Type Ik
Congenital Disorder of Glycosylation, Type Il
Congenital Disorder of Glycosylation, Type Im
Congenital Disorder of Glycosylation, Type in
Congenital Disorder of Glycosylation, Type Io
Congenital Disorder of Glycosylation, Type Ip
Congenital Disorder of Glycosylation, Type Iq
Congenital Disorder of Glycosylation, Type Ir
Congenital Disorder of Glycosylation, Type It
Congenital Disorder of Glycosylation, Type Iu
Congenital Disorder of Glycosylation, Type Iw
Congenital Disorder of Glycosylation, Type Ix
Congenital Disorder of Glycosylation, Type Iy
Congenital Erosive and Vesicular Dermatosis
Congenital Generalized Lipodystrophy
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
Congenital Ichthyosiform Erythroderma
Congenital Ichthyosis-Microcephalus-Tetraplegia Syndrome
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Congenital Panfollicular Nevus
Congenital Smooth Muscle Hamartoma
Conjunctival Pigmentation
Conjunctival Squamous Cell Carcinoma
Conotruncal Heart Malformations
Contact Dermatitis
Contagious Pustular Dermatitis
Coproporphyria, Hereditary
Cornea Squamous Cell Carcinoma
Corneodermatoosseous Syndrome
Corticosteroid-Sensitive Aseptic Abscesses
Costello Syndrome
Cowden Disease
Cowden Syndrome 1
Cowden Syndrome 2
Cowden Syndrome 3
Cowden Syndrome 4
Cowden Syndrome 5
Cowden Syndrome 6
Cowden Syndrome 7
Crandall Syndrome
Cranioectodermal Dysplasia 1
Cranioectodermal Dysplasia 2
Cranioectodermal Dysplasia 3
Cranioectodermal Dysplasia 4
Craniofaciofrontodigital Syndrome
Crest Syndrome
Curly Hair-Acral Keratoderma-Caries Syndrome
Curry-Jones Syndrome
Cutaneous Adenocystic Carcinoma
Cutaneous Anthrax
Cutaneous Diphtheria
Cutaneous Fibrous Histiocytoma
Cutaneous Ganglioneuroma
Cutaneous Leiomyosarcoma
Cutaneous Liposarcoma
Cutaneous Lupus Erythematosus
Cutaneous Mastocytoma
Cutaneous Mucoepidermoid Carcinoma
Cutaneous Pseudolymphoma
Cutaneous Solitary Mastocytoma
Cutaneous T Cell Lymphoma
Cutaneous Telangiectasia and Cancer Syndrome, Familial
Cutaneus Colagenous Vasculopathy
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
Cutis Marmorata Telangiectatica Congenita
Cutis Verticis Gyrata
Cylindromatosis, Familial
Cystic Basal Cell Carcinoma
Cytophagic Histiocytic Panniculitis
Daentl Towsend Siegel Syndrome
Darier-White Disease
Deafness, Conductive, with Ptosis and Skeletal Anomalies
Deafness, Congenital, with Onychodystrophy, Autosomal Dominant
Deafness, Congenital, with Total Albinism
Deafness Enamel Hypoplasia Nail Defects
Deafness, Neural, with Atypical Atopic Dermatitis
De Barsy Syndrome
Decubitus Ulcer
Deep Dermatophytosis
Degos 'en Cocarde' Erythrokeratoderma
Dermal Ridges, Nelson Syndrome
Dermal Ridges-off-the-End
Dermal Ridges, Patternless
Dermal Unilateral Segmental Cavernous Angioma
Dermatitis
Dermatitis, Atopic
Dermatitis, Atopic, 2
Dermatitis, Atopic, 3
Dermatitis, Atopic, 4
Dermatitis, Atopic, 5
Dermatitis, Atopic, 6
Dermatitis, Atopic, 7
Dermatitis, Atopic, 8
Dermatitis, Atopic, 9
Dermatitis Herpetiformis
Dermatitis Herpetiformis, Familial
Dermatocardioskeletal Syndrome Boronne Type
Dermato-Cardio-Skeletal Syndrome, Borrone Type
Dermatofibrosarcoma Protuberans
Dermatoglyphics--Arch on Any Digit
Dermatoglyphics--Fingerprint Pattern
Dermatoglyphics--Finger Ridge Count
Dermatoglyphics--Hypothenar Radial Arch
Dermatoglyphics--Palmar Triradius D, Absence of
Dermatographia
Dermatoleukodystrophy
Dermatomycosis
Dermatomyositis
Dermatoosteolysis, Kirghizian Type
Dermatopathia Pigmentosa Reticularis
Dermatophytosis
Dermatosis Papulosa Nigra
Dermochondrocorneal Dystrophy
Dermographism, Familial
Dermoid Cyst of Skin
Dermoodontodysplasia
Dermotrichic Syndrome
Didymosis Aplasticosebacea
Diffuse Cutaneous Mastocytosis
Diffuse Cutaneous Systemic Sclerosis
Diffuse Dermal Angiomatosis
Diffuse Leptomeningeal Melanocytosis
Diffuse Lipomatosis
Diffuse Palmoplantar Keratoderma-Acrocyanosis Syndrome
Diffuse Palmoplantar Keratoderma, Bothnian Type
Diffuse Scleroderma
Digestive System Melanoma
Digital Clubbing, Isolated Congenital
Discoid Fibromas, Familial Multiple
Discoid Lupus Erythematosus
Discrete Papular Lichen Myxedematosus
Dominant Dystrophic Epidermolysis Bullosa
Dominant Dystrophic Epidermolysis Bullosa, Nails Only
Dominant Ichthyosis Vulgaris
Donohue Syndrome
Dowling-Degos Disease
Dowling-Degos Disease 1
Dowling-Degos Disease 2
Dowling-Degos Disease 3
Dowling-Degos Disease 4
Drug-Induced Lupus Erythematosus
Drug Rash with Eosinophilia and Systemic Symptoms
Dubowitz Syndrome
Dwarfism with Stiff Joints and Ocular Abnormalities
Dyschromatosis Symmetrica Hereditaria
Dyschromatosis Universalis Hereditaria
Dyschromatosis Universalis Hereditaria 1
Dyschromatosis Universalis Hereditaria 2
Dyschromatosis Universalis Hereditaria 3
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
Dysmorphism Cleft Palate Loose Skin
Dysplastic Nevus Syndrome
Eccrine Acrospiroma
Eccrine Adenocarcinoma
Eccrine Mixed Tumor of Skin
Eccrine Papillary Adenocarcinoma
Eccrine Papillary Adenoma
Eccrine Porocarcinoma
Eccrine Sweat Gland Neoplasm
Ecthyma
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 4, Hair/nail Type
Ectodermal Dysplasia 5, Hair/nail Type
Ectodermal Dysplasia 6, Hair/nail Type
Ectodermal Dysplasia 7, Hair/nail Type
Ectodermal Dysplasia 8, Hair/tooth/nail Type
Ectodermal Dysplasia 9, Hair/nail Type
Ectodermal Dysplasia and Neurosensory Deafness
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy Syndrome
Ectodermal Dysplasia, Hidrotic, Christianson-Fourie Type
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia
Ectodermal Dysplasia/short Stature Syndrome
Ectodermal Dysplasia/skin Fragility Syndrome
Ectodermal Dysplasia-Syndactyly Syndrome 1
Ectodermal Dysplasia-Syndactyly Syndrome 2
Ectodermal Dysplasia, Trichoodontoonychial Type
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type
Eczema Herpeticum
Eczematous Dermatitis of Eyelid
Ehlers-Danlos/osteogenesis Imperfecta Syndrome
Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome, Arthrochalasia Type, 1
Ehlers-Danlos Syndrome, Arthrochalasia Type, 2
Ehlers-Danlos Syndrome, Cardiac Valvular Type
Ehlers-Danlos Syndrome, Classic-Like
Ehlers-Danlos Syndrome, Classic Type, 1
Ehlers-Danlos Syndrome, Classic Type, 2
Ehlers-Danlos Syndrome, Dermatosparaxis Type
Ehlers-Danlos Syndrome, Hypermobility Type
Ehlers-Danlos Syndrome, Kyphoscoliotic Form
Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1
Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 2
Ehlers-Danlos Syndrome, Musculocontractural Type, 1
Ehlers-Danlos Syndrome, Musculocontractural Type, 2
Ehlers-Danlos Syndrome, Periodontal Type, 1
Ehlers-Danlos Syndrome, Periodontal Type, 2
Ehlers-Danlos Syndrome Progeroid Type
Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1
Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2
Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3
Ehlers-Danlos Syndrome Type 2
Ehlers-Danlos Syndrome, Type V
Ehlers-Danlos Syndrome, Vascular-Like Type
Ehlers-Danlos Syndrome, Vascular Type
Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality
Elastoderma
Elastofibroma Dorsi
Elastoma
Elastosis Perforans Serpiginosa
Elliott Ludman Teebi Syndrome
Ellis-Van Creveld Syndrome
Encephalocraniocutaneous Lipomatosis
Encephalopathy, Progressive, with or Without Lipodystrophy
Endometriosis in Scar of Skin
Epidermal Appendage Tumor
Epidermal Nevus Vitamin D Resistant Rickets
Epidermodysplasia Verruciformis
Epidermodysplasia Verruciformis, X-Linked
Epidermoid Brain Cyst
Epidermoid Cysts
Epidermolysa Bullosa Simplex with Muscular Dystrophy
Epidermolysis Bullosa
Epidermolysis Bullosa Acquisita
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Dystrophica, Autosomal Dominant
Epidermolysis Bullosa Dystrophica, Autosomal Recessive
Epidermolysis Bullosa Dystrophica Neurotrophica
Epidermolysis Bullosa Dystrophica, Pretibial
Epidermolysis Bullosa, Junctional, Herlitz Type
Epidermolysis Bullosa Junctionalis with Pyloric Atresia
Epidermolysis Bullosa, Junctional, Non-Herlitz Type
Epidermolysis Bullosa, Late-Onset Localized Junctional, with Mental Retardation
Epidermolysis Bullosa, Lethal Acantholytic
Epidermolysis Bullosa, Nonspecific, Autosomal Recessive
Epidermolysis Bullosa Pruriginosa
Epidermolysis Bullosa Simplex
Epidermolysis Bullosa Simplex, Autosomal Recessive 1
Epidermolysis Bullosa Simplex, Autosomal Recessive 2
Epidermolysis Bullosa Simplex, Dowling-Meara Type
Epidermolysis Bullosa Simplex, Generalized
Epidermolysis Bullosa Simplex, Generalized, with Scarring and Hair Loss
Epidermolysis Bullosa Simplex, Localized
Epidermolysis Bullosa Simplex, Ogna Type
Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex with Anodontia/hypodontia
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema
Epidermolysis Bullosa Simplex with Mottled Pigmentation
Epidermolysis Bullosa Simplex with Muscular Dystrophy
Epidermolysis Bullosa Simplex with Nail Dystrophy
Epidermolysis Bullosa Simplex with Pyloric Atresia
Epidermolysis Bullosa with Congenital Localized Absence of Skin and Deformity of Nails
Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase
Epidermolysis Bullosa with Diaphragmatic Hernia
Epidermolysis Bullosa with Pyloric Atresia
Epidermolytic Acanthoma
Epidermolytic Hyperkeratosis
Epidermolytic Nevus
Epithelioid Cell Melanoma
Erdheim-Chester Disease
Erosive Pustular Dermatosis of the Scalp
Erysipelas
Erythema Elevatum Diutinum
Erythema Infectiosum
Erythema Multiforme
Erythema Palmare Hereditarium
Erythematosquamous Dermatosis
Erythrasma
Erythroderma, Congenital, with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-Ige
Erythroderma Desquamativa of Leiner
Erythroderma, Ichthyosiform, Congenital Reticular
Erythroderma, Lethal Congenital
Erythrokeratodermia-Cardiomyopathy Syndrome
Erythrokeratodermia Variabilis Et Progressiva 1
Erythrokeratodermia Variabilis Et Progressiva 2
Erythrokeratodermia Variabilis Et Progressiva 3
Erythrokeratodermia Variabilis Et Progressiva 4
Erythrokeratodermia Variabilis Et Progressiva 5
Erythromelalgia
Erythropoietic Uroporphyria Associated with Myeloid Malignancy
Esophageal Cancer
Esophagus Melanoma
Ethmoid Sinus Squamous Cell Carcinoma
Exanthem
Exfoliative Dermatitis
Exfoliative Ichthyosis
External Ear Squamous Cell Carcinoma
Extranodal Nasal Nk/t Cell Lymphoma
Extrasystoles, Multiform Ventricular, with Short Stature, Hyperpigmentation and Microcephaly
Eyebrows, Duplication of, with Stretchable Skin and Syndactyly
Fabry Disease
Facial Dermatosis
Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome
Familial Adenomatous Polyposis
Familial Adenomatous Polyposis 1
Familial Adenomatous Polyposis 2
Familial Adenomatous Polyposis 3
Familial Adenomatous Polyposis 4
Familial Anetoderma
Familial Candidiasis
Familial Chilblain Lupus
Familial Cold Autoinflammatory Syndrome
Familial Cold Autoinflammatory Syndrome 1
Familial Cold Autoinflammatory Syndrome 2
Familial Cold Autoinflammatory Syndrome 3
Familial Cold Autoinflammatory Syndrome 4
Familial Keratoacanthoma
Familial Partial Lipodystrophy
Familial Partial Lipodystrophy Due to Akt2 Mutations
Familial Pityriasis Rubra Pilaris
Familial Porphyria Cutanea Tarda
Familial Progressive Hyperpigmentation
Familial Short Qt Syndrome
Familial Tumoral Calcinosis
Fanconi Anemia, Complementation Group a
Fanconi Anemia, Complementation Group D1
Fanconi Anemia, Complementation Group D2
Fanconi Anemia, Complementation Group E
Fanconi Anemia, Complementation Group F
Fanconi Anemia, Complementation Group I
Fanconi Anemia, Complementation Group J
Fanconi Anemia, Complementation Group L
Fanconi Anemia, Complementation Group N
Fanconi Anemia, Complementation Group O
Fanconi Anemia, Complementation Group P
Fanconi Anemia, Complementation Group Q
Fanconi Anemia, Complementation Group R
Fanconi Anemia, Complementation Group T
Fanconi Anemia, Complementation Group U
Fanconi Anemia, Complementation Group V
Fanconi Anemia, Complementation Group W
Farber Lipogranulomatosis
Fibrodysplasia Ossificans Progressiva
Fibroepithelial Polyp of the Anus
Fibroepithelial Polyp of Urethra
Fixed Pigmented Erythema
Flotch Syndrome
Flynn-Aird Syndrome
Focal Acral Hyperkeratosis
Focal Dermal Hypoplasia
Focal Facial Dermal Dysplasia
Focal Facial Dermal Dysplasia 1, Brauer Type
Focal Facial Dermal Dysplasia 2, Brauer-Setleis Type
Focal Facial Dermal Dysplasia 3, Setleis Type
Focal Facial Dermal Dysplasia 4
Focal Palmoplantar and Gingival Keratoderma
Follicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts
Follicular Mucinosis
Folliculitis
Folliculotropic Mycosis Fungoides
Fontaine Progeroid Syndrome
Fox-Fordyce Disease
Frank-Ter Haar Syndrome
Frontal Fibrosing Alopecia
Frontal Sinus Squamous Cell Carcinoma
Frontonasal Dysplasia 1
Frontonasal Dysplasia 2
Frontonasal Dysplasia 3
Gallbladder Melanoma
Gallbladder Squamous Cell Carcinoma
Gapo Syndrome
Gardner-Diamond Syndrome
Garret Tripp Syndrome
Gastrocutaneous Syndrome
Gaucher Disease, Perinatal Lethal
Generalized Eruptive Histiocytosis
Generalized Eruptive Keratoacanthoma
Generalized Peeling Skin Syndrome
Genuine Diffuse Phlebectasia
German Syndrome
Geroderma Osteodysplastica
Geroderma Osteodysplasticum
Gianotti Crosti Syndrome
Giant Congenital Nevus
Glottis Squamous Cell Carcinoma
Gomez-Lopez-Hernandez Syndrome
Gonadal Dysgenesis
Gorlin-Chaudhry-Moss Syndrome
Graham-Little-Piccardi-Lassueur Syndrome
Granuloma Annulare
Granulomatous Dermatitis
Granulomatous Disease, Chronic, Autosomal Dominant Type
Granulomatous Disease with Defect in Neutrophil Chemotaxis
Granulomatous Slack Skin Disease
Griscelli Syndrome
Griscelli Syndrome, Type 1
Griscelli Syndrome, Type 2
Griscelli Syndrome, Type 3
Grover's Disease
Growth Factors, Combined Defect of
Grubben De Cock Borghgraef Syndrome
Guttate Psoriasis
Haim-Munk Syndrome
Hair-an Syndrome
Hair Defect with Photosensitivity and Mental Retardation
Hair Disease
Hairy Elbows
Hairy Palms and Soles
Halal Setton Wang Syndrome
Hallermann-Streiff-Like Syndrome
Hallermann-Streiff Syndrome
Halo Nevi
Hand Dermatosis
Hartnup Disorder
Hemangioma, Capillary Infantile
Hemangioma of Subcutaneous Tissue
Hemihyperplasia-Multiple Lipomatosis Syndrome
Hennekam Syndrome
Hereditary Acrokeratotic Poikiloderma, Weary Type
Hereditary Angioedema
Hereditary Hemorrhagic Telangiectasia
Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary Sensorimotor Neuropathy with Hyperelastic Skin
Hereditary Sensory and Autonomic Neuropathy Type 1e
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 Gestationis
Herpetiform Pemphigus
Hidradenitis
Hidradenitis Suppurativa
Hidradenoma
Hidrocystoma
Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features
Histiocytic Dermatoarthritis
Histiocytosis, Progressive Mucinous
Holocarboxylase Synthetase Deficiency
Human T-Cell Leukemia Virus Type 1
Human T-Cell Leukemia Virus Type 2
Human T-Cell Leukemia Virus Type 3
Huriez Syndrome
Hutchinson-Gilford Progeria Syndrome
Hyaline Fibromatosis Syndrome
Hydroa Vacciniforme
Hydroa Vacciniforme, Familial
Hyper-Igd Syndrome
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant
Hyper-Ige Recurrent Infection Syndrome, Autosomal Recessive
Hyperkeratosis-Hyperpigmentation Syndrome
Hyperkeratosis Lenticularis Perstans
Hyperpigmentation, Familial Progressive, 1
Hyperpigmentation of Eyelids
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive
Hypertrichosis
Hypertrichosis, Anterior Cervical
Hypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy
Hypertrichosis, Congenital Generalized, with or Without Gingival Hyperplasia
Hypertrichosis Lanuginosa, Acquired
Hypertrichosis Lanuginosa Congenita
Hypertrichosis Universalis Congenita, Ambras Type
Hypertrophic or Verrucous Lupus Erythematosus
Hypertrophic Scars
Hypo- and Hypermelanotic Cutaneous Macules-Retarded Growth-Intellectual Disability Syndrome
Hypohidrosis
Hypohidrosis with Abnormal Palmar Dermal Ridges
Hypohidrotic Ectodermal Dysplasia Autosomal Recessive
Hypohidrotic Ectodermal Dysplasia with Immunodeficiency
Hypomelanosis of Ito
Hypopigmentation of Eyelid
Hypotrichosis and Recurrent Skin Vesicles
Hypotrichosis, Congenital, with Juvenile Macular Dystrophy
Hypotrichosis-Deafness Syndrome
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome
Hypotrichosis Simplex
Hypotrichosis Simplex of the Scalp
Ichthyosiform Erythroderma, Corneal Involvement, and Deafness
Ichthyosis
Ichthyosis, Acquired
Ichthyosis Bullosa of Siemens
Ichthyosis, Congenital, Autosomal Recessive 1
Ichthyosis, Congenital, Autosomal Recessive 10
Ichthyosis, Congenital, Autosomal Recessive 11
Ichthyosis, Congenital, Autosomal Recessive 12
Ichthyosis, Congenital, Autosomal Recessive 13
Ichthyosis, Congenital, Autosomal Recessive 14
Ichthyosis, Congenital, Autosomal Recessive 2
Ichthyosis, Congenital, Autosomal Recessive 3
Ichthyosis, Congenital, Autosomal Recessive 4a
Ichthyosis, Congenital, Autosomal Recessive 4b
Ichthyosis, Congenital, Autosomal Recessive 5
Ichthyosis, Congenital, Autosomal Recessive 6
Ichthyosis, Congenital, Autosomal Recessive 7
Ichthyosis, Congenital, Autosomal Recessive 8
Ichthyosis, Congenital, Autosomal Recessive 9
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
Ichthyosis, Hepatosplenomegaly, and Cerebellar Degeneration
Ichthyosis Hystrix, Curth-Macklin Type
Ichthyosis Hystrix Gravior
Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin
Ichthyosis Prematurity Syndrome
Ichthyosis, Spastic Quadriplegia, and Mental Retardation
Ichthyosis Vulgaris
Ichthyosis with Alopecia, Eclabium, Ectropion, and Mental Retardation
Ichthyosis, X-Linked
Ifap Syndrome with or Without Bresheck Syndrome
Immunodeficiency 11b with Atopic Dermatitis
Impetigo
Impetigo Herpetiformis
Incontinentia Pigmenti
Indeterminate Cell Histiocytosis
Infantile Digital Fibromatosis
Infantile Myofibromatosis
Infantile Onset Panniculitis with Uveitis and Systemic Granulomatosis
Infantile-Onset Periodic Fever-Panniculitis-Dermatosis Syndrome
Infective Dermatitis Associated with Htlv-1
Infiltrative Basal Cell Carcinoma
Inflamed Seborrheic Keratosis
Inflammatory Linear Verrucous Epidermal Nevus
Inflammatory Skin and Bowel Disease, Neonatal, 1
Inflammatory Skin and Bowel Disease, Neonatal, 2
Integumentary System Benign Neoplasm
Integumentary System Cancer
Intermediate Cell Type Ciliary Body Melanoma
Interstitial Granulomatous Dermatitis with Arthritis
Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital
Intraocular Melanoma
Inverted Follicular Keratosis
Iris Mixed Cell Melanoma
Iris Spindle Cell Melanoma
Irritant Dermatitis
Jessner Lymphocytic Infiltration of the Skin
Johanson-Blizzard Syndrome
Johnson Neuroectodermal Syndrome
Joint Laxity, Familial
Jones Hersh Yusk Syndrome
Judge Misch Wright Syndrome
Junctional Epidermolysis Bullosa
Junctional Epidermolysis Bullosa Inversa
Juvenile Dermatitis Herpetiformis
Juvenile Xanthogranuloma
Keppen-Lubinsky Syndrome
Keratinizing Squamous Cell Carcinoma
Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
Keratoacanthoma
Keratoderma Palmoplantaris Transgrediens
Keratoderma Palmoplantar Spastic Paralysis
Keratoderma, Palmoplantar, with Deafness
Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy
Keratoderma with Woolly Hair
Keratolytic Winter Erythema
Keratosis
Keratosis, Familial Actinic
Keratosis, Focal Palmoplantar and Gingival
Keratosis Follicularis, Dwarfism, and Cerebral Atrophy
Keratosis Follicularis Spinulosa Decalvans
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
Keratosis Palmaris Et Plantaris with Clinodactyly
Keratosis Palmoplantaris Striata Ii
Keratosis Palmoplantaris Striata Iii
Keratosis Pilaris Atrophicans
Keratosis, Seborrheic
Kerion Celsi
Kernicterus
Kernicterus Due to Isoimmunization
Kid Syndrome
Kimura Disease
Kindler Syndrome
Klippel-Trenaunay-Weber Syndrome
Knuckle Pads, Leuconychia and Sensorineural Deafness
Knuckle Pads, Leukonychia, and Sensorineural Deafness
Kohlschutter-Tonz Syndrome
Kosaki Overgrowth Syndrome
Kuzniecky Andermann Syndrome
Kwashiorkor
Kyphoscoliotic Ehlers-Danlos Syndrome
Lacrimal Gland Squamous Cell Carcinoma
Lacrimoauriculodentodigital Syndrome
Large Cell Carcinoma
Laryngoonychocutaneous Syndrome
Late-Onset Focal Dermal Elastosis
Late-Onset Junctional Epidermolysis Bullosa
Late-Onset Localized Junctional Epidermolysis Bullosa-Intellectual Disability Syndrome
Ledderhose Disease
Leg Dermatosis
Legius Syndrome
Leiomyoma Cutis
Leishmaniasis
Lelis Syndrome
Lentiginosis, Inherited Patterned
Lentigo Maligna Melanoma
Leukemia, B-Cell, Chronic
Leukemia, T-Cell, Chronic
Leukoencephalopathy Palmoplantar Keratoderma
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis
Leukomelanoderma Mental Redardation Hypotrichosis
Leukonychia Totalis-Acanthosis-Nigricans-Like Lesions-Abnormal Hair Syndrome
Lichen Amyloidosis
Lichen Disease
Lichen Nitidus
Lichen Planopilaris
Lichen Planus
Lichen Planus, Familial
Lichen Planus Pemphigoides
Lichen Planus Pigmentosus
Lichen Sclerosus Et Atrophicus
Limb-Mammary Syndrome
Limited Scleroderma
Linear Atrophoderma of Moulin
Linear Focal Elastosis
Linear Iga Disease
Linear Lichen Planus
Linear Scleroderma
Linear Skin Defects with Multiple Congenital Anomalies 1
Linear Skin Defects with Multiple Congenital Anomalies 2
Linear Skin Defects with Multiple Congenital Anomalies 3
Linear Verrucous Nevus Syndrome
Lipedema
Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy
Lipodermatosclerosis
Lipodystrophy
Lipodystrophy, Congenital Generalized, Type 1
Lipodystrophy, Congenital Generalized, Type 2
Lipodystrophy, Congenital Generalized, Type 3
Lipodystrophy, Congenital Generalized, Type 4
Lipodystrophy Due to Peptidic Growth Factors Deficiency
Lipodystrophy, Familial Partial, Type 1
Lipodystrophy, Familial Partial, Type 2
Lipodystrophy, Familial Partial, Type 3
Lipodystrophy, Familial Partial, Type 4
Lipodystrophy, Familial Partial, Type 5
Lipodystrophy, Familial Partial, Type 6
Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones
Lipodystrophy, Partial, Acquired
Lipoid Proteinosis of Urbach and Wiethe
Lipomatosis
Lipomatosis, Multiple
Lipomatosis, Multiple Symmetric
Lissencephaly
Lissencephaly 1
Lissencephaly 2
Lissencephaly 3
Lissencephaly 4
Lissencephaly 5
Lissencephaly 8
Livedoid Vasculopathy
Lmna-Related Cardiocutaneous Progeria Syndrome
Localized Junctional Epidermolysis Bullosa, Non-Herlitz Type
Localized Lichen Myxedematosus with Mixed Features of Different Subtypes
Localized Lichen Myxedematosus with Monoclonal Gammopathy or Systemic Symptoms
Localized Lipodystrophy
Localized Pagetoid Reticulosis
Localized Scleroderma
Loiasis
Loose Anagen Hair Syndrome
Ludwig's Angina
Lung Squamous Cell Carcinoma
Lupus Erythematosus
Lupus Erythematosus Panniculitis
Lupus Erythematosus Tumidus
Lymphadenitis
Lymphangiosarcoma
Lymphedema and Cerebral Arteriovenous Anomaly
Lymphedema, Cardiac Septal Defects, and Characteristic Facies
Lymphedema-Hypoparathyroidism Syndrome
Lymphedema, Primary, with Myelodysplasia
Lymphomatoid Papulosis
Macroepiphyseal Dysplasia with Osteoporosis, Wrinkled Skin, and Aged Appearance
Macs Syndrome
Macular Amyloidosis
Majeed Syndrome
Mal De Meleda
Malignant Acrospiroma
Malignant Anus Melanoma
Malignant Atrophic Papulosis
Malignant Breast Melanoma
Malignant Choroid Melanoma
Malignant Ciliary Body Melanoma
Malignant Conjunctival Melanoma
Malignant Cornea Melanoma
Malignant Eyelid Melanoma
Malignant Granular Cell Skin Tumor
Malignant Iris Melanoma
Malignant Melanoma, Childhood
Malignant Melanoma of the Mucosa
Malignant Skin Fibrous Histiocytoma
Malignant Spindle Cell Melanoma
Malignant Spiradenoma
Malignant Syringoma
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome
Mandibuloacral Dysplasia with Type a Lipodystrophy
Mandibuloacral Dysplasia with Type B Lipodystrophy
Mandibulofacial Dysostosis with Alopecia
Marie Unna Congenital Hypotrichosis
Marshall Syndrome
Mast Cell Disease
Mastocytosis Cutaneous with Short Stature Conductive Hearing Loss and Microtia
Maxillary Sinus Cholesteatoma
Maxillary Sinus Squamous Cell Carcinoma
Mccune-Albright Syndrome
Mediastinal Lipomatosis
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome
Megarbane-Jalkh Syndrome
Melanoacanthoma
Melanocytic Nevus Syndrome, Congenital
Melanoma
Melanoma-Associated Retinopathy
Melanoma-Astrocytoma Syndrome
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, Malignant Familial Intraocular
Melanoma Metastasis
Melanoma of Soft Tissue
Melanoma-Pancreatic Cancer Syndrome
Melanomatosis
Melanoma Tumor Antigen Gp90
Melanoma, Uveal
Melanoma, Uveal 1
Melanoma, Uveal 2
Melanosis, Neurocutaneous
Melkersson-Rosenthal Syndrome
Meningeal Melanoma
Meningeal Melanomatosis
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, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma
Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies
Merkel Cell Carcinoma
Mesomelic Dysplasia Skin Dimples
Metaphyseal Dysplasia, Anetoderma, and Optic Atrophy
Metaphyseal Modeling Abnormality, Skin Lesions, and Spastic Paraplegia
Metatypical Basal Cell Carcinoma
Mevalonic Aciduria
Microcephalic Primordial Dwarfism, Montreal Type
Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis
Micronodular Basal Cell Carcinoma
Mid-Dermal Elastolysis
Middle Ear Squamous Cell Carcinoma
Miliaria
Miliaria Rubra
Milner Khallouf Gibson Syndrome
Minimal Pigment Oculocutaneous Albinism Type 1
Mixed Cell Uveal Melanoma
Moloney Syndrome
Mongolian Spot
Monilethrix
Muckle-Wells Syndrome
Mucoepithelial Dysplasia, Hereditary
Mucopolysaccharidosis Iii
Mucopolysaccharidosis Iv
Mucopolysaccharidosis-Plus Syndrome
Mucopolysaccharidosis Type 2, Attenuated Form
Mucopolysaccharidosis Type 2, Severe Form
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
Mucosal Melanoma
Muir-Torre Syndrome
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly
Multicentric Reticulohistiocytosis
Multiple Benign Circumferential Skin Creases on Limbs
Multiple Enchondromatosis, Maffucci Type
Multiple Familial Trichoepithelioma
Multiple Fibrofolliculoma Familial
Multiple Sclerosis-Ichthyosis-Factor Viii Deficiency Syndrome
Multiple Self-Healing Squamous Epithelioma
Multiple Sulfatase Deficiency
Multiple Symmetrical Lipomatosis
Muscular Dystrophy, Congenital, Davignon-Chauveau Type
Musculocontractural Ehlers-Danlos Syndrome
Mycosis Fungoides
Myofibromatosis, Infantile, 1
Myofibromatosis, Infantile, 2
Myxofibrosarcoma
Naegeli-Franceschetti-Jadassohn Syndrome
Naegeli-Franceschetti-Jadassohn Syndrome/dermatopathia Pigmentosa Reticularis
Nail Disease
Nail Disorder, Nonsyndromic Congenital, 1
Nail Disorder, Nonsyndromic Congenital, 10
Nail Disorder, Nonsyndromic Congenital, 2
Nail Disorder, Nonsyndromic Congenital, 3
Nail Disorder, Nonsyndromic Congenital, 4
Nail Disorder, Nonsyndromic Congenital, 5
Nail Disorder, Nonsyndromic Congenital, 6
Nail Disorder, Nonsyndromic Congenital, 7
Nail Disorder, Nonsyndromic Congenital, 8
Nail Disorder, Nonsyndromic Congenital, 9
Nail-Patella Syndrome
Naxos Disease
Necrobiosis Lipoidica
Necrobiotic Xanthogranuloma
Necrotic Uveal Melanoma
Nelson Syndrome
Neonatal Dermatomyositis
Neonatal Inflammatory Skin and Bowel Disease
Neonatal Jaundice
Neonatal Scleroderma
Nephrogenic Systemic Fibrosis
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
Nestor-Guillermo Progeria Syndrome
Netherton Syndrome
Neu-Laxova Syndrome 1
Neurilemmomatosis
Neurodermatitis
Neurofibromatosis-Noonan Syndrome
Neurofibromatosis, Type I
Neurofibromatosis, Type Ii
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
Neuropathy, Hereditary, with or Without Age-Related Macular Degeneration
Neurotic Excoriation
Neutrophilic Dermatosis, Acute Febrile
Nevada Syndrome
Nevoid Hypermelanosis, Linear and Whorled
Nevus Comedonicus
Nevus, Epidermal
Nevus of Ota
Nodular Basal Cell Carcinoma
Nodular Cutaneous Amyloidosis
Nodular Hidradenoma
Nodular Lichen Myxedematosus
Nodular Malignant Melanoma
Nodular Nonsuppurative Panniculitis
Nodular Urticaria Pigmentosa
Noninfectious Dermatoses of Eyelid
Nonphotosensitive Trichothiodystrophy
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-Like Disorder with Loose Anagen Hair 1
Noonan Syndrome-Like Disorder with Loose Anagen Hair 2
Noonan Syndrome with Multiple Lentigines
Occipital Horn Syndrome
Occupational Dermatitis
Ocular Cicatricial Pemphigoid
Ocular Melanoma
Oculocerebral Syndrome with Hypopigmentation
Oculocerebrocutaneous Syndrome
Oculocutaneous Albinism
Oculodentodigital Dysplasia
Oculodentodigital Dysplasia, Autosomal Recessive
Oculodentodigital Dysplasia Dominant
Oculoectodermal Syndrome
Oculotrichodysplasia
Odontomicronychial Dysplasia
Odontoonychodermal Dysplasia
Odonto Onycho Dysplasia with Alopecia
Odontotrichoungual-Digital-Palmar Syndrome
Oliver-Mcfarlane Syndrome
Onychocytic Matricoma
Onychodystrophy-Anonychia
Onychomatricoma
Oral and Digital Anomalies with Ichthyosis
Oral Erosive Lichen
Orbital Melanoma
Osseous Heteroplasia, Progressive
Osteomyelitis, Sterile Multifocal, with Periostitis and Pustulosis
Osteopathia Striata with Pigmentary Dermopathy Including White Forelock
Osteopoikilosis
Osteosclerosis with Ichthyosis and Premature Ovarian Failure
Otoonychoperoneal Syndrome
Ovarian Melanoma
Pachyonychia Congenita 1
Pachyonychia Congenita 2
Pachyonychia Congenita 3
Pachyonychia Congenita 4
Pachyonychia Congenita, Autosomal Recessive
Paget Disease, Extramammary
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal
Palmoplantar Keratoderma and Congenital Alopecia 1
Palmoplantar Keratoderma and Congenital Alopecia 2
Palmoplantar Keratoderma and Woolly Hair
Palmoplantar Keratoderma, Bothnian Type
Palmoplantar Keratoderma, Epidermolytic
Palmoplantar Keratoderma I, Striate, Focal, or Diffuse
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques, X-Linked
Palmoplantar Keratoderma, Nagashima Type
Palmoplantar Keratoderma, Nonepidermolytic
Palmoplantar Keratoderma, Nonepidermolytic, Focal 1
Palmoplantar Keratoderma, Nonepidermolytic, Focal 2
Palmoplantar Keratoderma, Nonepidermolytic, Focal or Diffuse
Palmoplantar Keratoderma, Norrbotten Recessive Type
Palmoplantar Keratoderma of Sybert
Palmoplantar Keratoderma, Punctate Type Ia
Palmoplantar Keratoderma, Punctate Type Ib
Palmoplantar Keratoderma, Punctate Type Ii
Palmoplantar Keratoderma, Punctate Type Iii
Palmoplantar Keratoderma-Sclerodactyly Syndrome
Palmoplantar Keratosis
Panniculitis
Papillary Hidradenoma
Papillary Squamous Carcinoma
Papillon-Lefevre Syndrome
Papular Elastorrhexis
Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome
Papular Mucinosis
Papular Mucinosis of Infancy
Papular Xanthoma
Parana Hard-Skin Syndrome
Paranasal Sinus Cancer
Paranasal Sinus Cancer, Adult
Paraneoplastic Pemphigus
Parapsoriasis
Parc Syndrome
Parkes Weber Syndrome
Partial Deep Dermal and Full Thickness Burns
Pectus Excavatum, Macrocephaly, Short Stature, and Dysplastic Nails
Pediatric Leptomeningeal Melanoma
Peeling Skin Syndrome
Peeling Skin Syndrome 1
Peeling Skin Syndrome 2
Peeling Skin Syndrome 3
Peeling Skin Syndrome 4
Peeling Skin Syndrome 5
Peeling Skin Syndrome Type C
Peeling Skin with Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads
Peho-Like Syndrome
Peho Syndrome
Pellagra
Pellagra-Like Syndrome
Pelvic Lipomatosis
Pemphigoid Gestationis
Pemphigus
Pemphigus and Fogo Selvagem
Pemphigus Erythematosus
Pemphigus Foliaceus
Pemphigus Vegetans
Pemphigus Vulgaris
Pemphigus Vulgaris, Familial
Penis Squamous Cell Carcinoma
Perianal Skin Paget's Disease
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
Perinatal Jaundice Due to Hepatocellular Damage
Periodic Fever, Familial, Autosomal Dominant
Periodontal Ehlers-Danlos Syndrome
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
Periventricular Nodular Heterotopia
Periventricular Nodular Heterotopia 1
Periventricular Nodular Heterotopia 6
Periventricular Nodular Heterotopia 7
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
Phacomatosis Pigmentovascularis
Phakomatosis Cesioflammea
Phakomatosis Cesiomarmorata
Phakomatosis Pigmentokeratotica
Phakomatosis Spilorosea
Photoallergic Dermatitis
Photoparoxysmal Response 1
Photoparoxysmal Response 2
Photoparoxysmal Response 3
Phototoxic Dermatitis
Physical Urticaria
Piebald Trait
Piebald Trait with Neurologic Defects
Pierpont Syndrome
Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome
Pigmentation Disease
Pigmented Basal Cell Carcinoma
Pigmented Purpuric Dermatosis
Pili Bifurcati
Pili Gemini
Pili Torti
Pili Torti and Developmental Delay
Pili Torti, Early-Onset
Pili Torti Onychodysplasia
Pilodental Dysplasia with Refractive Errors
Pilomatrix Carcinoma
Pilomatrixoma
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities
Pinheiro Freire-Maia Miranda Syndrome
Pituitary Dermoid and Epidermoid Cysts
Pityriasis Lichenoides Chronica
Pityriasis Lichenoides Et Varioliformis Acuta
Pityriasis Rosea
Pityriasis Rubra Pilaris
Plantar Verrucous Skin Carcinoma
Plaque-Form Urticaria Pigmentosa
Poems Syndrome
Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Poikiloderma, Hereditary Sclerosing
Poikiloderma with Neutropenia
Polydactyly, Postaxial, Type A1
Polydactyly, Postaxial, Type A2
Polydactyly, Postaxial, Type A3
Polydactyly, Postaxial, Type A4
Polydactyly, Postaxial, Type A5
Polydactyly, Postaxial, Type A6
Polydactyly, Postaxial, Type A7
Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes
Pompholyx
Porokeratosis
Porokeratosis 1, Multiple Types
Porokeratosis 2, Palmar, Plantar, and Disseminated Type
Porokeratosis 3, Multiple Types
Porokeratosis 6, Multiple Types
Porokeratosis 7, Multiple Types
Porokeratosis 9, Multiple Types
Porokeratotic Eccrine Ostial and Dermal Duct Nevus
Porphyria, Acute Hepatic
Porphyria, Acute Intermittent
Porphyria, Congenital Erythropoietic
Porphyria Cutanea Tarda
Porphyria Cutanea Tarda, Type I
Porphyria Variegata
Postaxial Polydactyly of Toes
Posterior Uveal Melanoma
Premature Aging Syndrome, Penttinen Type
Primary Anetoderma
Primary Cutaneous Aggressive Epidermotropic Cd8+ T-Cell Lymphoma
Primary Cutaneous Amyloidosis
Primary Cutaneous Anaplastic Large Cell Lymphoma
Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma
Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type
Primary Cutaneous Follicle Center Lymphoma
Primary Cutaneous Gamma/delta-Positive T-Cell Lymphoma
Primary Cutaneous Marginal Zone B-Cell Lymphoma
Primary Cutaneous Peripheral T-Cell Lymphoma Not Otherwise Specified
Primary Cutaneous Plasmacytosis
Primary Essential Cutis Verticis Gyrata
Primary Malignant Melanoma of the Cervix
Primary Malignant Melanoma of the Conjunctiva
Primary Melanoma of the Central Nervous System
Progeroid Short Stature with Pigmented Nevi
Progeroid Syndrome, Neonatal
Progressive Nodular Histiocytosis
Prolidase Deficiency
Proliferating Trichilemmal Cyst
Proteus-Like Syndrome
Proteus Syndrome
Protoporphyria, Erythropoietic
Protoporphyria, Erythropoietic, X-Linked
Prurigo Nodularis
Pruritic Urticarial Papules and Plaques of Pregnancy
Pseudoatrophoderma Colli
Pseudofolliculitis Barbae
Pseudohypoparathyroidism
Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ib
Pseudohypoparathyroidism, Type Ic
Pseudohypoparathyroidism, Type Ii
Pseudopelade of Brocq
Pseudopseudohypoparathyroidism
Pseudosarcomatous Fibromatosis
Pseudovascular Skin Squamous Cell Carcinoma
Pseudoxanthoma Elasticum
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis
Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa
Pseudoxanthomatous Diffuse Cutaneous Mastocytosis
Psoriasis
Psoriasis 1
Psoriasis 10
Psoriasis 11
Psoriasis 12
Psoriasis 13
Psoriasis 14, Pustular
Psoriasis 15, Pustular
Psoriasis 2
Psoriasis 3
Psoriasis 4
Psoriasis 5
Psoriasis 6
Psoriasis 7
Psoriasis 8
Psoriasis 9
Psoriatic Arthritis
Pterygium, Antecubital
Punctate Acrokeratoderma Freckle Like Pigmentation
Punctate Palmoplantar Keratoderma
Punctate Porokeratosis
Pustular Psoriasis
Pustulosis of Palm and Sole
Pustulosis Palmaris Et Plantaris
Pyoderma
Pyoderma Gangrenosum
Pyoderma Gangrenosum-Acne-Suppurative Hidradenitis Syndrome
Pyogenic Arthritis, Pyoderma Gangrenosum and Acne
Pyogenic Granuloma
Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne
Quinquaud's Decalvans Folliculitis
Rare Lichen Planus
Recessive Dystrophic Epidermolysis Bullosa
Recessive Dystrophic Epidermolysis Bullosa-Generalized Other
Rectum Malignant Melanoma
Red Skin Pigment Anomaly of New Guinea
Refsum Disease, Classic
Renal Pelvis Squamous Cell Carcinoma
Restrictive Dermopathy, Lethal
Reticulate Acropigmentation of Kitamura
Retinal Melanoma
Reynolds Syndrome
Ringed Hair
Ritter's Disease
Roch-Leri Mesosomatous Lipomatosis
Rodrigues Blindness
Rombo Syndrome
Rosacea
Rosai-Dorfman Disease
Rothmund-Thomson Syndrome
Rothmund-Thomson Syndrome Type 1
Rothmund-Thomson Syndrome Type 2
Roy Maroteaux Kremp Syndrome
Russell-Silver Syndrome, X-Linked
Ruvalcaba Churesigaew Myhre Syndrome
Salivary Gland Adenoid Cystic Carcinoma
Salt and Pepper Developmental Regression Syndrome
Sapho Syndrome
Sarcomatoid Basal Cell Carcinoma
Sarcomatoid Squamous Cell Skin Carcinoma
Satoyoshi Syndrome
Scalp Defects and Postaxial Polydactyly
Scalp Dermatosis
Scalp Syndrome
Scarf Syndrome
Schimmelpenning-Feuerstein-Mims Syndrome
Schopf-Schulz-Passarge Syndrome
Scleredema
Scleredema Adultorum
Scleroderma, Familial Progressive
Scleromyxedema
Scleromyxedema Without Monoclonal Gammopathy
Scrotum Melanoma
Sebaceous Adenocarcinoma
Sebaceous Adenoma
Sebaceous Basal Cell Carcinoma
Sebaceous Gland Disease
Seborrhea-Like Dermatitis with Psoriasiform Elements
Seborrheic Dermatitis
Seborrheic Infantile Dermatitis
Segmental Outgrowth-Lipomatosis-Arteriovenous Malformation-Epidermal Nevus Syndrome
Self-Healing Papular Mucinosis
Self-Improving Collodion Baby
Senile Angioma
Sequeiros Sack Syndrome
Severe Cutaneous Adverse Reaction
Sezary's Disease
Shaheen Syndrome
Short Qt Syndrome
Short Qt Syndrome 1
Short Qt Syndrome 2
Short Qt Syndrome 3
Short Syndrome
Signet Ring Basal Cell Carcinoma
Sjogren-Larsson-Like Syndrome
Sjogren-Larsson Syndrome
Skin Amelanotic Melanoma
Skin Angiosarcoma
Skin Atrophy
Skin Benign Neoplasm
Skin Cancer, Non Melanoma, Childhood
Skin Carcinoma in Situ
Skin Conditions
Skin Creases, Congenital Symmetric Circumferential, 1
Skin Creases, Congenital Symmetric Circumferential, 2
Skin Disease
Skin Epithelioid Hemangioma
Skin Fragility-Woolly Hair-Palmoplantar Keratoderma Syndrome
Skin Fragility-Woolly Hair Syndrome
Skin Glomangioma
Skin Glomus Tumor
Skin Granular Cell Tumor
Skin/hair/eye Pigmentation, Variation in, 1
Skin/hair/eye Pigmentation, Variation in, 10
Skin/hair/eye Pigmentation, Variation in, 11
Skin/hair/eye Pigmentation, Variation in, 2
Skin/hair/eye Pigmentation, Variation in, 3
Skin/hair/eye Pigmentation, Variation in, 5
Skin/hair/eye Pigmentation, Variation in, 6
Skin/hair/eye Pigmentation, Variation in, 7
Skin/hair/eye Pigmentation, Variation in, 8
Skin/hair/eye Pigmentation, Variation in, 9
Skin Hemangioma
Skin Lipoma
Skin Melanoma
Skin Meningioma
Skin Papilloma
Skin Pilomatrix Carcinoma
Skin Sarcoidosis
Skin Sarcoma
Skin Squamous Cell Carcinoma
Skint1-Like Pseudogene
Skin Tag
Small Cell Carcinoma
Small Cell Sarcoma
Sneddon Syndrome
Solar Urticaria
Sparse Hair-Short Stature-Skin Anomalies Syndrome
Spastic Paraplegia with Neuropathy and Poikiloderma
Sphenoid Sinus Squamous Cell Carcinoma
Spinal Cord Melanoma
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 Type 16
Spinocerebellar Ataxia Type 19/22
Spiradenoma
Split-Foot Malformation with Mesoaxial Polydactyly
Spondylodysplastic Ehlers-Danlos Syndrome
Spondyloepimetaphyseal Dysplasia with Joint Laxity, Type 1, with or Without Fractures
Spongiotic Dermatitis
Squamous Cell Carcinoma
Squamous Cell Papilloma
Squamous Cell Papilloma of Skin
Steatocystoma Multiplex
Steatocystoma Multiplex with Natal Teeth
Steroid Lipomatosis
Stiff Skin Syndrome
Sting-Associated Vasculopathy, Infantile-Onset
Striate Palmoplantar Keratoderma
Stromal Corneal Pigmentation
Sturge-Weber Syndrome
Subacute Cutaneous Lupus Erythematosus
Subcorneal Pustular Dermatosis
Subcutaneous Panniculitis-Like T-Cell Lymphoma
Subglottis Squamous Cell Carcinoma
Superficial Spreading Melanoma
Supraglottis Squamous Cell Carcinoma
Sweat Gland Cancer
Sweat Gland Disease
Syringocystadenoma Papilliferum
Syringoma
Syringomas, Multiple
Systemic Lupus Erythematosus
Systemic Lupus Erythematosus 1
Systemic Lupus Erythematosus 10
Systemic Lupus Erythematosus 11
Systemic Lupus Erythematosus 12
Systemic Lupus Erythematosus 13
Systemic Lupus Erythematosus 14
Systemic Lupus Erythematosus 15
Systemic Lupus Erythematosus 16
Systemic Lupus Erythematosus 2
Systemic Lupus Erythematosus 3
Systemic Lupus Erythematosus 4
Systemic Lupus Erythematosus 5
Systemic Lupus Erythematosus 6
Systemic Lupus Erythematosus 7
Systemic Lupus Erythematosus 8
Systemic Lupus Erythematosus 9
Systemic Scleroderma
Takenouchi-Kosaki Syndrome
Tang Hsi Ryu Syndrome
T-Cell Immunodeficiency with Epidermodysplasia Verruciformis
T-Cell Leukemia
Teebi-Shaltout Syndrome
Teeth, Congenital Absence of, with Taurodontia and Sparse Hair
Telangiectasia, Hereditary Benign
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
Telangiectasia Macularis Eruptiva Perstans
Telfer Sugar Jaeger Syndrome
Telogen Effluvium
Temple-Baraitser Syndrome
Terminal Osseous Dysplasia
Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities
Thumb Deformity, Alopecia, Pigmentation Anomaly
Thymus Squamous Cell Carcinoma
Tièche-Jadassohn Nevus
Tietz Albinism-Deafness Syndrome
Tinea Barbae
Tinea Capitis
Tinea Corporis
Tinea Cruris
Tinea Manuum
Tinea Pedis
Tinea Profunda
Tinea Unguium
Toxicodendron Dermatitis
Trachea Squamous Cell Carcinoma
Transient Bullous Dermolysis of the Newborn
Trichodental Dysplasia
Trichodentoosseous Syndrome
Trichodysplasia-Amelogenesis Imperfecta Syndrome
Trichodysplasia-Xeroderma
Trichoepithelioma, Multiple Familial, 1
Trichoepithelioma, Multiple Familial, 2
Trichofolliculoma
Trichomegaly
Trichoodontoonychial Dysplasia with Bone Deficiency
Tricho Odonto Onycho Dermal Syndrome
Trichorhinophalangeal Syndrome
Trichorhinophalangeal Syndrome Type 1 and 3
Trichorhinophalangeal Syndrome, Type I
Trichorhinophalangeal Syndrome, Type Ii
Trichorhinophalangeal Syndrome, Type Iii
Trichothiodystrophy 1, Photosensitive
Trichothiodystrophy 2, Photosensitive
Trichothiodystrophy 3, Photosensitive
Trichothiodystrophy 4, Nonphotosensitive
Trichothiodystrophy 5, Nonphotosensitive
Trichothiodystrophy 6, Nonphotosensitive
Tuberculin Skin Test Reactivity, Absence of
Tuberculin Skin Test Reactivity Quantitative Trait Locus
Tuberous Sclerosis
Tuberous Sclerosis 1
Tuberous Sclerosis 2
Tumoral Calcinosis, Hyperphosphatemic, Familial
Tumoral Calcinosis, Normophosphatemic, Familial
Tylosis with Esophageal Cancer
Type I Ehlers-Danlos Syndrome
Typical Urticaria Pigmentosa
Tyrosinemia
Tyrosinemia, Type I
Tyrosinemia, Type Ii
Tyrosinemia, Type Iii
Ulcer of Lower Limbs
Ulerythema Ophryogenesis
Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and Brachydactyly
Uncombable Hair Syndrome 1
Uncombable Hair Syndrome 2
Uncombable Hair Syndrome 3
Unna-Thost Palmoplantar Keratoderma
Ureter Squamous Cell Carcinoma
Urethra Squamous Cell Carcinoma
Urticaria
Uveal Epithelioid Cell Melanoma
Uv-Sensitive Syndrome
Uv-Sensitive Syndrome 1
Uv-Sensitive Syndrome 2
Uv-Sensitive Syndrome 3
Van Den Bosch Syndrome
Vascular Skin Disease
Verruciform Xanthoma of Skin
Verrucous Nevus Acanthokeratolytic
Vesiculobullous Skin Disease
Vibratory Urticaria
Vici Syndrome
Viral Exanthem
Virus-Associated Trichodysplasia Spinulosa
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1
Vohwinkel Syndrome
Vohwinkel Syndrome, Variant Form
Vulva Fibroepithelial Polyp
Vulvar Inverted Follicular Keratosis
Vulvar Melanoma
Vulvar Seborrheic Keratosis
Vulva Squamous Cell Carcinoma
Vulvovaginal Gingival 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
Warty Dyskeratoma
Weill-Marchesani-Like Syndrome
Weill-Marchesani Syndrome
Weill-Marchesani Syndrome 1
Weill-Marchesani Syndrome 2
Weill-Marchesani Syndrome 3
Wells Syndrome
Werner Syndrome
Weyers Acrofacial Dysostosis
White Fibrous Papulosis of the Neck
White Sponge Nevus 1
White Sponge Nevus 2
Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 2
Wiskott-Aldrich Syndrome, Autosomal Dominant Form
Witkop Syndrome
Woolly Hair, Autosomal Dominant
Woolly Hair, Autosomal Recessive 3
Woolly Hair, Hypotrichosis, Everted Lower Lip, and Outstanding Ears
Woolly Hair Syndrome
Wound Botulism
Wrinkly Skin Syndrome
Wyburn Mason's Syndrome
Xanthoma Disseminatum
Xeroderma of Eyelid
Xeroderma Pigmentosum, Autosomal Dominant, Mild
Xeroderma Pigmentosum, Complementation Group a
Xeroderma Pigmentosum, Complementation Group B
Xeroderma Pigmentosum, Complementation Group C
Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group E
Xeroderma Pigmentosum, Complementation Group F
Xeroderma Pigmentosum, Complementation Group G
Xeroderma Pigmentosum Group E
Xeroderma Pigmentosum, Type 2
Xeroderma Pigmentosum, Type 9
Xeroderma Pigmentosum, Variant Type
Xeroderma Talipes Enamel Defects
X-Linked Chondrodysplasia Punctata
X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome
X-Linked Keloid Scarring-Reduced Joint Mobility-Increased Optic Cup-to-Disc Ratio Syndrome
Yellow Nail Syndrome
Yemenite Deaf-Blind Hypopigmentation Syndrome
Yusho Disease
Zinc, Elevated Plasma
Zinc-Responsive Necrolytic Acral Erythema |
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