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| Boli A-Z | | 3mc Syndrome
Aapoai Amyloidosis
Aapoaii Amyloidosis
Aapoaiv Amyloidosis
Acquired Central Diabetes Insipidus
Acquired Cutis Laxa
Acquired Cystic Disease-Associated Renal Cell Carcinoma
Acquired Fructose Intolerance
Acquired Monoclonal Ig Light Chain-Associated Fanconi Syndrome
Acquired Pseudoxanthoma Elasticum
Acropectororenal Dysplasia
Acro-Pectoro-Renal Field Defect
Acrorenal-Mandibular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome, Autosomal Recessive
Acrorenal Syndrome Recessive
Acute Conjunctivitis
Acute Cystitis
Acute Diffuse Nephritis
Acute Gonococcal Cystitis
Acute Kidney Failure
Acute Kidney Tubular Necrosis
Acute Poststreptococcal Glomerulonephritis
Acute Proliferative Glomerulonephritis
Acute Pyelonephritis
Acute Urate Nephropathy
Adenine Phosphoribosyltransferase Deficiency
Adrenocortical Carcinoma, Hereditary
Adult Dermatomyositis
Adult Familial Nephronophthisis-Spastic Quadriparesia Syndrome
Adult Malignant Mesenchymoma
Adult Mesoblastic Nephroma
Adult-Onset Still's Disease
Afib Amyloidosis
Ah Amyloidosis
Alagille Syndrome 1
Alagille Syndrome 2
Al Amyloidosis
Allain-Babin-Demarquez Syndrome
Alpha-1-Antitrypsin Deficiency
Alpha-Thalassemia
Alport Syndrome and Thin Basement Membrane Nephropathy
Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Recessive
Alport Syndrome, X-Linked
Alsing Syndrome
Alstrom Syndrome
Amelogenesis Imperfecta
Amelogenesis Imperfecta Hypoplastic Type, Ig
Amelogenesis Imperfecta Type 2a1
Amelogenesis Imperfecta, Type Ia
Amelogenesis Imperfecta, Type Ib
Amelogenesis Imperfecta, Type Ic
Amelogenesis Imperfecta, Type Ie
Amelogenesis Imperfecta, Type if
Amelogenesis Imperfecta, Type Ig
Amelogenesis Imperfecta, Type Ih
Amelogenesis Imperfecta, Type Iiia
Amelogenesis Imperfecta, Type Iiib
Amelogenesis Imperfecta, Type Iv
Amyloidosis
Amyloidosis Aa
Amyloidosis, Familial Visceral
Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps
Aniridia, Partial, with Unilateral Renal Agenesis and Psychomotor Retardation
Aniridia Renal Agenesis Psychomotor Retardation
Antenatal Bartter Syndrome
Anterior Urethral Valve
Anti-Basement Membrane Glomerulonephritis
Anuria
Apparent Mineralocorticoid Excess
Aredyld
Arthrogryposis, Renal Dysfunction, and Cholestasis 1
Arthrogryposis, Renal Dysfunction, and Cholestasis 2
Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
Atresia of Urethra
Atypical Hemolytic-Uremic Syndrome with H Factor Anomaly
Autoimmune Interstitial Lung, Joint, and Kidney Disease
Autosomal Dominant Polycystic Kidney Disease
Autosomal Dominant Proximal Renal Tubular Acidosis
Autosomal Dominant Tubulointerstitial Kidney Disease
Autosomal Dominant Tubulointerstitial Kidney Disease, Muc1-Related
Autosomal Dominant Tubulointerstitial Kidney Disease, Ren-Related
Autosomal Dominant Tubulointerstitial Kidney Disease, Umod-Related
Autosomal Recessive Hypophosphatemic Rickets
Autosomal Recessive Malignant Osteopetrosis
Axial Mesodermal Dysplasia Spectrum
Bacterial Conjunctivitis
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
Bartter Disease
Bartter Syndrome, Type 1, Antenatal
Bartter Syndrome, Type 2, Antenatal
Bartter Syndrome, Type 3
Bartter Syndrome Type 4
Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness
Bartter Syndrome, Type 4b, Neonatal, with Sensorineural Deafness
Bartter Syndrome, Type 5, Antenatal, Transient
Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome Due to 11p15 Microdeletion
Beckwith-Wiedemann Syndrome Due to 11p15 Microduplication
Beckwith-Wiedemann Syndrome Due to 11p15 Translocation/inversion
Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15
Beckwith-Wiedemann Syndrome Due to Paternal Uniparental Disomy of Chromosome 11
Behcet Syndrome
Ben Ari Shuper Mimouni Syndrome
Benign Hypertensive Renal Disease
Benign Mesenchymoma
Benign Metanephric Tumour
Beta-Amino Acids, Renal Transport of
Beta-Aminoisobutyric Aciduria
Beta-Thalassemia
Beta-Thalassemia, Dominant Inclusion Body Type
Bifid Nose with or Without Anorectal and Renal Anomalies
Bilateral Multicystic Dysplastic Kidney
Bilateral Renal Agenesis Dominant Type
Bilateral Renal Aplasia
Biliary Malformation with Renal Tubular Insufficiency
Billet Bear Syndrome
Birt-Hogg-Dube Syndrome
Bk-Virus Nephropathy
Bladder Adenocarcinoma
Bladder Benign Neoplasm
Bladder Calculus
Bladder Cancer
Bladder Cancer, Childhood
Bladder Carcinoma in Situ
Bladder Clear Cell Adenocarcinoma
Bladder Colloid Adenocarcinoma
Bladder Colonic Type Adenocarcinoma
Bladder Diffuse Clear Cell Adenocarcinoma
Bladder Disease
Bladder Diverticulum
Bladder Dome Cancer
Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex
Bladder Flat Intraepithelial Lesion
Bladder Hepatoid Adenocarcinoma
Bladder Lateral Wall Cancer
Bladder Leiomyoma
Bladder Lymphoma
Bladder Mixed Adenocarcinoma
Bladder Neck Cancer
Bladder Neck Obstruction
Bladder Papillary Clear Cell Adenocarcinoma
Bladder Papillary Transitional Cell Neoplasm
Bladder Sarcoma
Bladder Signet Ring Cell Adenocarcinoma
Bladder Squamous Cell Carcinoma
Bladder Squamous Papilloma
Bladder Transitional Cell Papilloma
Bladder Trigone Cancer
Bladder Tuberculosis
Bladder Tubulo-Cystic Clear Cell Adenocarcinoma
Bladder Urachal Adenocarcinoma
Bladder Urachal Carcinoma
Bladder Urachal Squamous Cell Carcinoma
Bladder Urachal Urothelial Carcinoma
Bladder Urothelial Carcinoma
Bladder Urothelial Papillary Carcinoma
Bladder Verrucous Squamous Cell Carcinoma
Blastema Predominant Kidney Wilms' Tumor
Blue Diaper Syndrome
Brachymesomelia-Renal Syndrome
Brain Malformations with or Without Urinary Tract Defects
Branchiootorenal/branchiootic Syndrome
Branchiootorenal Spectrum Disorders
Branchiootorenal Syndrome
Branchiootorenal Syndrome 1
Branchiootorenal Syndrome 2
Buerger Disease
C1q Nephropathy
Cardiomyopathy-Renal Anomalies Syndrome
Carnitine Deficiency, Systemic Primary
Cataract
Cataract 10, Multiple Types
Cataract 11, Multiple Types
Cataract 12, Multiple Types
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 Congenital Autosomal Dominant
Cataract-Intellectual Disability-Anal Atresia-Urinary Defects Syndrome
Cataract, Total Congenital
Cat Eye Syndrome
Cellular Congenital Mesoblastic Nephroma
Central Nervous System Calcification-Deafness-Tubular Acidosis-Anemia Syndrome
Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula
Cfhr5 Deficiency
Charcot-Marie-Tooth Disease, Dominant Intermediate D
Charcot-Marie-Tooth Disease, Dominant Intermediate E
Charcot-Marie-Tooth Disease, Dominant Intermediate F
Charcot-Marie-Tooth Disease, Recessive Intermediate D
Childhood Kidney Angiomyolipoma
Childhood Kidney Cell Carcinoma
Childhood Multilocular Cystic Kidney Neoplasm
Childhood Type Dermatomyositis
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome
Chromophil Renal Cell Carcinoma
Chromophobe Renal Cell Carcinoma
Chromosome 16p13.3 Deletion Syndrome, Proximal
Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb
Chromosome 8q12.1-Q21.2 Deletion Syndrome
Chronic Conjunctivitis
Chronic Cystitis
Chronic Interstitial Cystitis
Chronic Kidney Failure
Chronic Pyelonephritis
Chronic Rapidly Progressive Glomerulonephritis
Classic Congenital Mesoblastic Nephroma
Classic Variant of Chromophobe Renal Cell Carcinoma
Clear Cell Papillary Renal Cell Carcinoma
Clear Cell Renal Cell Carcinoma
Clear Cell Variant Infiltrating Bladder Urothelial Carcinoma
Coenzyme Q10 Deficiency, Primary, 5
Coenzyme Q10 Deficiency, Primary, 6
Collagen Type Iii Glomerulopathy
Collecting Duct Carcinoma
Complement Factor H Deficiency
Congenital Anomalies of Kidney and Urinary Tract 1
Congenital Anomalies of Kidney and Urinary Tract 2
Congenital Anomalies of Kidney and Urinary Tract Syndrome with or Without Hearing Loss, Abnormal Ears, or Developmental Delay
Congenital Bilateral Megacalycosis
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 Megacalycosis
Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization
Congenital Mesoblastic Nephroma
Congenital Nephrotic Syndrome Finnish Type
Congenital Primary Megaureter
Congenital Primary Megaureter, Nonrefluxing and Unobstructed Form
Congenital Primary Megaureter, Obstructed Form
Congenital Primary Megaureter, Refluxing Form
Congenital Renal Artery Stenosis
Congenital Sialidosis Type 2
Conjunctivitis
Coproporphyria, Hereditary
Corpus Callosum Agenesis Double Urinary Collecting
Cranioectodermal Dysplasia 1
Cranioectodermal Dysplasia 2
Cranioectodermal Dysplasia 3
Cranioectodermal Dysplasia 4
Crescentic Glomerulonephritis
Crome Syndrome
Cryoglobulinemia, Familial Mixed
Cutaneous Polyarteritis Nodosa
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
Cystic Kidney Disease
Cystic Nephroma
Cystinosis
Cystinosis, Adult Nonnephropathic
Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type
Cystinosis, Nephropathic
Cystinuria
Cystitis
Daentl Towsend Siegel Syndrome
Daneman Davy Mancer Syndrome
Danubian Endemic Familial Nephropathy
Dent Disease 1
Dent Disease 2
Denys-Drash Syndrome
Dermatomyositis
Diabetes Insipidus
Diabetes Insipidus, Nephrogenic, Autosomal
Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification
Diabetes Insipidus, Nephrogenic, X-Linked
Diabetes Insipidus, Neurohypophyseal
Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
Diaphanospondylodysostosis
Dicarboxylic Aminoaciduria
Diffuse Cutaneous Systemic Sclerosis
Diffuse Glomerulonephritis
Diffuse Mesangial Sclerosis
Dihydrolipoamide Dehydrogenase Deficiency
Dominant Hypophosphatemia with Nephrolithiasis or Osteoporosis
Donnai-Barrow Syndrome
Double Uterus-Hemivagina-Renal Agenesis
D-Plus Hemolytic Uremic Syndrome
Drug-Related Renal Tubular Dysgenesis
Duane-Radial Ray Syndrome
Duplication of Urethra
Dyschondrosteosis and Nephritis
Ehlers-Danlos Syndrome, Musculocontractural Type, 1
Ehlers-Danlos Syndrome, Musculocontractural Type, 2
Ellis-Van Creveld Syndrome
Ellis Yale Winter Syndrome
End Stage Renal Failure
Eosinophilic Granulomatosis with Polyangiitis
Eosinophilic Variant of Chromophobe Renal Cell Carcinoma
Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure
Epispadias
Epithelial Predominant Wilms' Tumor
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract
Erythrocyte Galactose Epimerase Deficiency
Erythropoietic Uroporphyria Associated with Myeloid Malignancy
Erythropoietin Polycythemia
Exstrophy of Bladder
Exudative Glomerulonephritis
Fabry Disease
Faciocardiorenal Syndrome
Familial Hyperaldosteronism
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes
Familial Juvenile Hyperuricaemic Nephropathy
Familial Mediterranean Fever
Familial Mediterranean Fever, Autosomal Dominant
Familial Nephrotic Syndrome
Familial Porphyria Cutanea Tarda
Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia
Familial Renal Oncocytoma
Familial Renal Papillary Carcinoma
Familial Wilms Tumor 2
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
Fanconi-Bickel Syndrome
Fanconi-Like Syndrome
Fanconi Renotubular Syndrome 1
Fanconi Renotubular Syndrome 2
Fanconi Renotubular Syndrome 3
Fanconi Syndrome
Feigenbaum Bergeron Richardson Syndrome
Female Stress Incontinence
Fibrillary Glomerulonephritis
Fibuloulnar Aplasia or Hypoplasia with Renal Abnormalities
Fish-Eye Disease
Fitzsimmons Walson Mellor Syndrome
Focal Embolic Glomerulonephritis
Focal Segmental Glomerulosclerosis
Focal Segmental Glomerulosclerosis 1
Focal Segmental Glomerulosclerosis 2
Focal Segmental Glomerulosclerosis 3
Focal Segmental Glomerulosclerosis 4
Focal Segmental Glomerulosclerosis 5
Focal Segmental Glomerulosclerosis 6
Focal Segmental Glomerulosclerosis 7
Focal Segmental Glomerulosclerosis 8
Focal Segmental Glomerulosclerosis 9
Forsythe-Wakeling Syndrome
Fraser Jequier Chen Syndrome
Frasier Syndrome
Fructose Intolerance, Hereditary
Fryns Syndrome
Galactokinase Deficiency
Galactose Epimerase Deficiency
Galactosemia
Gall Bladder Carcinoma in Situ
Gallbladder Disease
Gallbladder Disease 1
Gallbladder Disease 2
Gallbladder Disease 3
Gallbladder Disease 4
Galloway-Mowat Syndrome
Galloway-Mowat Syndrome 1
Galloway-Mowat Syndrome 3
Galloway-Mowat Syndrome 4
Galloway-Mowat Syndrome 5
Generalized Galactose Epimerase Deficiency
Genitopatellar Syndrome
Gitelman Syndrome
Global Developmental Delay-Lung Cysts-Overgrowth-Wilms Tumor Syndrome
Glomerulonephritis
Glomerulopathy with Fibronectin Deposits 1
Glomerulopathy with Fibronectin Deposits 2
Glycogen Storage Disease
Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency
Glycogen Storage Disease Ia
Glycogen Storage Disease Ib
Glycogen Storage Disease Ic
Glycogen Storage Disease Ii
Glycogen Storage Disease Iii
Glycogen Storage Disease Iv
Glycogen Storage Disease Ix
Glycogen Storage Disease Ixa
Glycogen Storage Disease Ixb
Glycogen Storage Disease Ixc
Glycogen Storage Disease Type 0
Glycogen Storage Disease, Type Ixd
Glycogen Storage Disease V
Glycogen Storage Disease Vi
Glycogen Storage Disease Vii
Glycogen Storage Disease Viii
Glycogen Storage Disease X
Glycogen Storage Disease Xii
Glycogen Storage Disease Xiii
Glycogen Storage Disease Xv
Glycoprotein, Renal
Goiter, Multinodular, Cystic Renal Disease, and Digital Anomalies
Goodpasture Syndrome
Gorlin Bushkell Jensen Syndrome
Graham Boyle Troxell Syndrome
Green Sandford Davison Syndrome
Hartnup Disorder
Heavy Chain Deposition Disease
Hematuria, Benign Familial
Hemoglobinuria
Hemolytic-Uremic Syndrome
Hemolytic Uremic Syndrome, Atypical 1
Hemolytic Uremic Syndrome, Atypical 2
Hemolytic Uremic Syndrome, Atypical 3
Hemolytic Uremic Syndrome, Atypical 4
Hemolytic Uremic Syndrome, Atypical 5
Hemolytic Uremic Syndrome, Atypical 6
Hemorrhagic Fever with Renal Syndrome
Hepatorenal Syndrome
Hereditary Amyloidosis
Hereditary Central Diabetes Insipidus
Hereditary Conventional Renal Cell Carcinoma
Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke
Hereditary Hypophosphatemic Rickets
Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary Paraganglioma-Pheochromocytoma Syndromes
Hereditary Renal Cell Carcinoma
Hereditary Wilms' Tumor
Hereditary Xanthinuria
Hinman Syndrome
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness
Histidinemia
Histidinuria Due to a Renal Tubular Defect
Histidinuria Renal Tubular Defect
Holzgreve Syndrome
Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type
Hydronephrosis
Hyperaldosteronism, Familial, Type I
Hyperaldosteronism, Familial, Type Ii
Hyperaldosteronism, Familial, Type Iii
Hyperaldosteronism, Familial, Type Iv
Hyperglycinuria
Hyperoxaluria, Primary, Type I
Hyperoxaluria, Primary, Type Ii
Hyperoxaluria, Primary, Type Iii
Hyperparathyroidism 2 with Jaw Tumors
Hypertension and Brachydactyly Syndrome
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertensive Nephropathy
Hyperthyroidism, Familial Gestational
Hyperthyroidism, Nonautoimmune
Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation
Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome
Hyperuricemic Nephropathy, Familial Juvenile, 1
Hyperuricemic Nephropathy, Familial Juvenile, 2
Hyperuricemic Nephropathy, Familial Juvenile, 3
Hyperuricemic Nephropathy, Familial Juvenile, 4
Hypocalcemia, Autosomal Dominant 1
Hypocalcemia, Autosomal Dominant 2
Hypocomplementemic Urticarial Vasculitis
Hypogonadism-Cataract Syndrome
Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy
Hypomagnesemia 1, Intestinal
Hypomagnesemia 2, Renal
Hypomagnesemia 3, Renal
Hypomagnesemia 4, Renal
Hypomagnesemia 5, Renal, with Ocular Involvement
Hypomagnesemia 6, Renal
Hypoparathyroidism, Sensorineural Deafness, and Renal Disease
Hypophosphatemia, Renal, with Intracerebral Calcifications
Hypophosphatemic Rickets, Autosomal Dominant
Hypophosphatemic Rickets, Autosomal Recessive, 1
Hypophosphatemic Rickets, Autosomal Recessive, 2
Hypophosphatemic Rickets with Hypercalciuria, Hereditary
Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Recessive
Hypoplastic Amelogenesis Imperfecta
Hypotonia-Cystinuria Syndrome
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome
Hypotrichosis-Lymphedema-Telangiectasia Syndrome
Hypouricemia, Familial Renal, Due to Tubular Hypersecretion
Hypouricemia, Renal, 1
Hypouricemia, Renal, 2
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
Idiopathic Hypercalciuria
Idiopathic Infantile Hypercalcemia
Idiopathic Steroid-Sensitive Nephrotic Syndrome with Diffuse Mesangial Proliferation
Idiopathic Steroid-Sensitive Nephrotic Syndrome with Focal Segmental Hyalinosis
Idiopathic Steroid-Sensitive Nephrotic Syndrome with Minimal Change
Iga Glomerulonephritis
Iga Nephropathy 1
Iga Nephropathy 2
Iga Nephropathy 3
Igg4-Related Kidney Disease
Immune-Complex Glomerulonephritis
Immunoglobulin a Vasculitis
Immunotactoid Glomerulopathy
Impaired Renal Function Disease
Inborn Renal Aminoaciduria
Infantile Bartter Syndrome with Sensorineural Deafness
Infiltrating Bladder Lymphoepithelioma-Like Carcinoma
Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant
Infiltrating Renal Pelvis Transitional Cell Carcinoma
Infundibulopelvic Dysgenesis
Intermediate Maple Syrup Urine Disease
Interstitial Cystitis
Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital
Interstitial Nephritis
Interstitial Nephritis, Karyomegalic
Invasive Bladder Transitional Cell Carcinoma
Ischiadic Hypoplasia Renal Dysfunction Immunodeficiency
Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type
Jejunal Atresia with Renal Adysplasia
Jewett-Marshall Bladder Cancer
Joubert Syndrome 1
Joubert Syndrome 10
Joubert Syndrome 13
Joubert Syndrome 14
Joubert Syndrome 15
Joubert Syndrome 16
Joubert Syndrome 17
Joubert Syndrome 18
Joubert Syndrome 2
Joubert Syndrome 20
Joubert Syndrome 21
Joubert Syndrome 22
Joubert Syndrome 23
Joubert Syndrome 24
Joubert Syndrome 25
Joubert Syndrome 26
Joubert Syndrome 27
Joubert Syndrome 28
Joubert Syndrome 3
Joubert Syndrome 30
Joubert Syndrome 31
Joubert Syndrome 32
Joubert Syndrome 33
Joubert Syndrome 4
Joubert Syndrome 5
Joubert Syndrome 6
Joubert Syndrome 7
Joubert Syndrome 8
Joubert Syndrome 9
Joubert Syndrome with Oculorenal Anomalies
Joubert Syndrome with Renal Anomalies
Juvenile Polymyositis
Juvenile Sialidosis Type 2
Juvenile Temporal Arteritis
Kallikrein, Decreased Urinary Activity of
Karandikar Maria Kamble Syndrome
Kelley-Seegmiller Syndrome
Kidney Angiomyolipoma
Kidney Benign Neoplasm
Kidney Cancer
Kidney Carcinoma in Situ
Kidney Clear Cell Sarcoma
Kidney Cortex Necrosis
Kidney Disease
Kidney Hemangiopericytoma
Kidney Hypertrophy
Kidney Osteogenic Sarcoma
Kidney Papillary Necrosis
Kidney Pelvis Papillary Carcinoma
Kidney Pelvis Sarcomatoid Transitional Cell Carcinoma
Kidney Rhabdoid Cancer
Kidney Sarcoma
Korean Hemorrhagic Fever
Lachiewicz Sibley Syndrome
Langer Nishino Yamaguchi Syndrome
Late-Onset Nephronophthisis
Lecithin:cholesterol Acyltransferase Deficiency
Leigh Syndrome with Nephrotic Syndrome
Leiomyomatosis, Diffuse, with Alport Syndrome
Lesch-Nyhan Syndrome
Liddle Syndrome
Light and Heavy Chain Deposition Disease
Light Chain Deposition Disease
Limited Scleroderma
Lipid-Cell Variant Infiltrating Bladder Urothelial Carcinoma
Lipoid Nephrosis
Lipoprotein Glomerulopathy
Localized Scleroderma
Low Compliance Bladder
Lowe Oculocerebrorenal Syndrome
Lower Urinary Tract Calculus
Ltbp4-Related Cutis Laxa
Lubinsky Syndrome
Lupus Erythematosus
Lymphedema-Distichiasis Syndrome
Lymphoma-Like Variant Infiltrating Bladder Urothelial Carcinoma
Malignant Cystic Nephroma
Malignant Hypertensive Renal Disease
Malignant Mesenchymoma
Maple Syrup Urine Disease
Maple Syrup Urine Disease, Mild Variant
Mayer-Rokitansky-Kuster-Hauser Syndrome
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
Medullary Cystic Kidney Disease 1
Medullary Cystic Kidney Disease 2
Medullary Sponge Kidney
Megacystis-Megaureter Syndrome
Megaloblastic Anemia
Megaloblastic Anemia 1
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
Membranoproliferative Glomerulonephritis
Membranous Nephropathy
Mesangial Proliferative Glomerulonephritis
Mesangial Sclerosis, Diffuse Renal, with Ocular Abnormalities
Mesenchymoma
Methionine Malabsorption Syndrome
Methylmalonic Aciduria and Homocystinuria, Cbld Type
Methylmalonic Aciduria, Cbla Type
Methylmalonic Aciduria, Cblb Type
Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs
Microcystic Variant Infiltrating Bladder Urothelial Carcinoma
Micropapillary Variant Infiltrating Bladder Urothelial Carcinoma
Microscopic Polyangiitis
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
Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis
Mitochondrial Complex Iii Deficiency, Nuclear Type 1
Mitochondrial Dna Depletion Syndrome 8a
Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form
Mixed Cell Type Kidney Wilms' Tumor
Mixed Connective Tissue Disease
Mixed Cryoglobulinemia Type Iii
Mosaic Monosomy X
Mucinous Tubular and Spindle Renal Cell Carcinoma
Muckle-Wells Syndrome
Mullerian Aplasia
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly
Mullerian Duct Aplasia, Unilateral Renal Agenesis, and Cervicothoracic Somite Anomalies
Multicentric Carpotarsal Osteolysis Syndrome
Multicentric Osteolysis Nephropathy
Multicystic Dysplastic Kidney
Multilocular Clear Cell Renal Cell Carcinoma
Multilocular Cystic Renal Neoplasm of Low Malignant Potential
Multiloculated Renal Cyst
Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly
Murcs Association
Musculocontractural Ehlers-Danlos Syndrome
Myeloma, Multiple
Nail-Patella-Like Renal Disease
Nail-Patella Syndrome
Neonatal Urinary Tract Infectious Disease
Nephrocalcinosis
Nephrogenic Adenofibroma
Nephrogenic Adenoma
Nephrogenic Adenoma of the Urethra
Nephrogenic Adenoma of Urinary Bladder
Nephrogenic Syndrome of Inappropriate Antidiuresis
Nephrogenic Systemic Fibrosis
Nephrolithiasis
Nephrolithiasis, Calcium Oxalate
Nephrolithiasis/osteoporosis, Hypophosphatemic, 1
Nephrolithiasis/osteoporosis, Hypophosphatemic, 2
Nephrolithiasis, Uric Acid
Nephrolithiasis, X-Linked Recessive, with Renal Failure
Nephronophthisis
Nephronophthisis 1
Nephronophthisis 11
Nephronophthisis 12
Nephronophthisis 13
Nephronophthisis 14
Nephronophthisis 15
Nephronophthisis 16
Nephronophthisis 18
Nephronophthisis 19
Nephronophthisis 2
Nephronophthisis 20
Nephronophthisis 3
Nephronophthisis 4
Nephronophthisis 7
Nephronophthisis 9
Nephronophthisis Familial Adult Spastic Quadriparesis
Nephronophthisis-Like Nephropathy 1
Nephropathy, Chronic Tubulointerstitial
Nephropathy, Deafness, and Hyperparathyroidism
Nephropathy Familial with Hyperuricemia
Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease
Nephropathy, Progressive, with Deafness
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness
Nephrosclerosis
Nephrosialidosis
Nephrosis with Deafness and Urinary Tract and Digital Malformations
Nephrotic Syndrome
Nephrotic Syndrome 14
Nephrotic Syndrome 15
Nephrotic Syndrome 16
Nephrotic Syndrome, Idiopathic, Steroid-Resistant
Nephrotic Syndrome Ocular Anomalies
Nephrotic Syndrome, Type 1
Nephrotic Syndrome, Type 10
Nephrotic Syndrome, Type 11
Nephrotic Syndrome, Type 12
Nephrotic Syndrome, Type 13
Nephrotic Syndrome, Type 2
Nephrotic Syndrome, Type 3
Nephrotic Syndrome, Type 4
Nephrotic Syndrome, Type 5, with or Without Ocular Abnormalities
Nephrotic Syndrome, Type 6
Nephrotic Syndrome, Type 7
Nephrotic Syndrome, Type 8
Nephrotic Syndrome, Type 9
Nested Variant Infiltrating Bladder Urothelial Carcinoma
Neuraminidase Deficiency
Neuroaxonal Dystrophy Renal Tubular Acidosis
Neurofaciodigitorenal Syndrome
Neurofibromatosis, Type I
Neurofibromatosis, Type Ii
Neurogenic Bladder
Neuromuscular Disease
Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine
Neutropenia
Neutropenia, Chronic Familial
Neutropenia, Severe Congenital, 1, Autosomal Dominant
Neutropenia, Severe Congenital, 2, Autosomal Dominant
Neutropenia, Severe Congenital, 3, Autosomal Recessive
Neutropenia, Severe Congenital, 4, Autosomal Recessive
Neutropenia, Severe Congenital, 5, Autosomal Recessive
Neutropenia, Severe Congenital, 6, Autosomal Recessive
Neutropenia, Severe Congenital, 7, Autosomal Recessive
Noduli Cutanei, Multiple, with Urinary Tract Abnormalities
Non-Amyloid Monoclonal Immunoglobulin Deposition Disease
Non-Congenital Cyst of Kidney
Non-Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis
Non-Invasive Bladder Papillary Urothelial Neoplasm
Non-Invasive Bladder Urothelial Carcinoma
Non-Papillary Transitional Cell Carcinoma of the Bladder
Non-Renal Secondary Hyperparathyroidism
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
Oculo Skeletal Renal Syndrome
Oeis Complex
Oligomeganephronic Renal Hypoplasia
Olivopontocerebellar Atrophy
Olivopontocerebellar Atrophy Ii, Autosomal Recessive
Olivopontocerebellar Atrophy V
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
Orthostatic Proteinuria
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
Papillorenal Syndrome
Paroxysmal Nocturnal Hemoglobinuria
Paroxysmal Nocturnal Hemoglobinuria 1
Paroxysmal Nocturnal Hemoglobinuria 2
Patau Syndrome
Patent Urachus
Pauci-Immune Glomerulonephritis
Pauci-Immune Glomerulonephritis with Anca
Pauci-Immune Glomerulonephritis Without Anca
Pax2-Related Disorder
Pediatric Systemic Lupus Erythematosus
Pelvic Lipomatosis with Crossed Renal Ectopia
Perinephritis
Perlman Syndrome
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
Phosphoribosylpyrophosphate Synthetase Superactivity
Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction
Pierson Syndrome
Plasmacytoid Variant Infiltrating Bladder Urothelial Carcinoma
Polyarteritis Nodosa
Polycystic Kidney Disease
Polycystic Kidney Disease 1
Polycystic Kidney Disease 2
Polycystic Kidney Disease 3
Polycystic Kidney Disease 4 with or Without Hepatic Disease
Polycystic Kidney Disease 5
Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis
Polymyositis
Polyomavirus Allograft Nephropathy
Porphyria, Acute Hepatic
Porphyria, Acute Intermittent
Porphyria, Congenital Erythropoietic
Porphyria Cutanea Tarda
Porphyria Cutanea Tarda, Type I
Porphyria Variegata
Posterior Urethral Valves
Potter's Syndrome
Primary Fanconi Syndrome
Primary Hyperoxaluria
Primary Localized Amyloidosis
Primary Megaureter, Adult-Onset Form
Primary Polyarteritis Nodosa
Proliferative Glomerulonephritis
Proteinuria, Low Molecular Weight, with Hypercalciuria and Nephrocalcinosis
Protoporphyria, Erythropoietic
Protoporphyria, Erythropoietic, X-Linked
Prune Belly Syndrome
Pseudohypoaldosteronism
Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type Iia
Pseudohypoaldosteronism, Type Iib
Pseudohypoaldosteronism, Type Iic
Pseudohypoaldosteronism, Type Iid
Pseudohypoaldosteronism, Type Iie
Pseudohypoparathyroidism
Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ib
Pseudohypoparathyroidism, Type Ic
Pseudohypoparathyroidism, Type Ii
Pseudopseudohypoparathyroidism
Pseudo-Turner Syndrome
Pseudoxanthoma Elasticum
Pulmonic Stenosis and Congenital Nephrosis
Pyelitis
Pyelonephritis
Pyeloureteritis Cystica
Pyuria
Radial-Renal Syndrome
Radiation Cystitis
Radio Renal Syndrome
Rapidly Progressive Glomerulonephritis
Relapsing Polychondritis
Renal Adenoma
Renal Adysplasia Dominant Type
Renal Agenesis, Bilateral
Renal Agenesis Meningomyelocele Mullerian Defect
Renal Agenesis, Unilateral
Renal and Mullerian Duct Hypoplasia
Renal Artery Atheroma
Renal Artery Disease
Renal Artery Obstruction
Renal Caliceal Diverticuli Deafness
Renal Carcinoma, Familial
Renal Cell Carcinoma 4
Renal Cell Carcinoma Associated with Neuroblastoma
Renal Cell Carcinoma, Nonpapillary
Renal Cell Carcinoma, Papillary, 1
Renal Cell Carcinoma, Xp11-Associated
Renal Clear Cell Carcinoma
Renal Cysts and Diabetes Syndrome
Renal Dysplasia
Renal Dysplasia, Bilateral
Renal Dysplasia, Cystic
Renal Dysplasia Diffuse Autosomal Recessive
Renal Dysplasia Diffuse Cystic
Renal Dysplasia-Limb Defects Syndrome
Renal Dysplasia, Unilateral
Renal Failure, Progressive, with Hypertension
Renal Fibrosis
Renal, Genital, and Middle Ear Anomalies
Renal Glucosuria
Renal-Hepatic-Pancreatic Dysplasia
Renal-Hepatic-Pancreatic Dysplasia 1
Renal-Hepatic-Pancreatic Dysplasia 2
Renal Hypertension
Renal Hypodysplasia/aplasia 1
Renal Hypodysplasia/aplasia 2
Renal Hypodysplasia/aplasia 3
Renal Hypoplasia
Renal Hypoplasia, Bilateral
Renal Hypoplasia, Unilateral
Renal Infectious Disease
Renal Nutcracker Syndrome
Renal Oncocytoma
Renal Osteodystrophy
Renal Pelvis Adenocarcinoma
Renal Pelvis Carcinoma
Renal Pelvis Inverted Papilloma
Renal Pelvis Squamous Cell Carcinoma
Renal Pelvis Transitional Cell Carcinoma
Renal Pelvis Urothelial Papilloma
Renal Tuberculosis
Renal Tubular Acidosis
Renal Tubular Acidosis, Distal
Renal Tubular Acidosis, Distal, Autosomal Dominant
Renal Tubular Acidosis, Distal, Autosomal Recessive
Renal Tubular Acidosis, Distal, Type 3
Renal Tubular Acidosis, Distal, Type 4
Renal Tubular Acidosis, Distal, with Hemolytic Anemia
Renal Tubular Acidosis, Distal, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness
Renal Tubular Acidosis Iii
Renal Tubular Acidosis, Proximal
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation
Renal Tubular Dysgenesis
Renal Tubular Dysgenesis Due to Twin-Twin Transfusion
Renal Tubular Transport Disease
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna
Ren-Related Kidney Disease
Reynolds Syndrome
Rhyns Syndrome
Right Atrial Isomerism
Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction
Rrm2b-Related Mitochondrial Dna Depletion Syndrome
Rrm2b-Related Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Renal Tubulopathy
Rubinstein Taybi Like Syndrome
Rubinstein-Taybi Syndrome 1
Rubinstein-Taybi Syndrome 2
Sacral Defect with Anterior Meningocele
Saito Kuba Tsuruta Syndrome
Salcedo Syndrome
Santos Mateus Leal Syndrome
Sarcoidosis 1
Sarcoidosis 2
Sarcoidosis 3
Sarcomatoid Renal Cell Carcinoma
Schimke Immunoosseous Dysplasia
Scleroderma, Familial Progressive
Secondary Hyperparathyroidism of Renal Origin
Secondary Polyarteritis Nodosa
Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance
Selig Benacerraf Greene Syndrome
Senior-Boichis Syndrome
Senior-Løken Syndrome
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
Severe Congenital Neutropenia
Severe Congenital Neutropenia Autosomal Dominant
Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly
Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly
Sickle Cell Anemia
Simpson-Golabi-Behmel Syndrome
Simpson-Golabi-Behmel Syndrome, Type 1
Simpson-Golabi-Behmel Syndrome, Type 2
Single-Organ Polyarteritis Nodosa
Slc4a1-Associated Distal Renal Tubular Acidosis
Small Cell Carcinoma of the Bladder
Smith-Lemli-Opitz Syndrome
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy
Split Hand Urinary Anomalies Spina Bifida
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects
Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Collapsing Glomerulopathy
Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Proliferation
Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis
Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Focal Segmental Hyalinosis
Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes
Steinfeld Syndrome
Stone in Bladder Diverticulum
Stricture or Kinking of Ureter
Stromal Predominant Kidney Wilms' Tumor
Stromme Syndrome
Structural Heart Defects and Renal Anomalies Syndrome
Subacute Glomerulonephritis
Superficial Urinary Bladder Cancer
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 Polyarteritis Nodosa
Systemic Scleroderma
Tafro Syndrome
Takayasu Arteritis
Tall Stature-Intellectual Disability-Renal Anomalies Syndrome
Temporal Arteritis
Thalassemia
Thrombocytopenia with Elevated Serum Iga and Renal Disease
Thrombotic Thrombocytopenic Purpura
Thrombotic Thrombocytopenic Purpura, Acquired
Thrombotic Thrombocytopenic Purpura, Congenital
Thymic-Renal-Anal-Lung Dysplasia
Thyrocerebroretinal Syndrome
Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations
Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia
Townes-Brocks Syndrome
Townes-Brocks Syndrome 1
Townes-Brocks Syndrome 2
Transient Pseudohypoaldosteronism
Transitional Cell Cancer of the Renal Pelvis and Ureter
Transitional Cell Carcinoma
Trigonitis
Tuberous Sclerosis
Tuberous Sclerosis 1
Tuberous Sclerosis 2
Tubular Renal Disease-Cardiomyopathy Syndrome
Tubulocystic Renal Cell Carcinoma
Tubulointerstitial Nephritis with Uveitis
Turner Syndrome
Turner Syndrome Due to Structural X Chromosome Anomalies
Type Ii Mixed Cryoglobulinemia
Tyrosinemia
Tyrosinemia, Type I
Tyrosinemia, Type Ii
Tyrosinemia, Type Iii
Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia
Unilateral Congenital Megacalycosis
Unilateral Multicystic Dysplastic Kidney
Urachal Cyst
Urachal Diverticulum
Urachal Sinus
Uremia
Uremic Neuropathy
Ureteric Orifice Cancer
Ureterolithiasis
Urethral Calculus
Urethral Diverticulum
Urethral Gland Abscess
Urethral Obstruction Sequence
Urethral Stricture
Urethral Syndrome
Urethritis
Urinary Bladder Anterior Wall Cancer
Urinary Bladder, Atony of
Urinary Bladder Inverted Papilloma
Urinary Bladder Posterior Wall Cancer
Urinary Bladder Small Cell Neuroendocrine Carcinoma
Urinary Bladder Villous Adenoma
Urinary Schistosomiasis
Urinary System Disease
Urinary Tract Infections, Recurrent
Urinary Tract Non-Invasive Transitional Cell Neoplasm
Urinary Tract Obstruction
Urinary Tract Papillary Transitional Cell Benign Neoplasm
Urofacial Syndrome 1
Urofacial Syndrome 2
Urolithiasis, Uric Acid, Autosomal Dominant
Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis
Vacterl Hydrocephaly
Vascular Cancer
Vascular Hyalinosis
Vasculopathy, Retinal, with Cerebral Leukodystrophy
Vater/vacterl Association
Velocardiofacial Syndrome
Ventriculomegaly with Cystic Kidney Disease
Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1
Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2
Visceral Myopathy
Vitamin B12-Responsive Methylmalonic Acidemia
Von Hippel-Lindau Syndrome
Webb-Dattani Syndrome
Wegener Granulomatosis
Williams-Beuren Syndrome
Wilms Tumor 1
Wilms Tumor 2
Wilms Tumor 3
Wilms Tumor 4
Wilms Tumor 5
Wilms Tumor 6
Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome
Wilson Disease
Xanthinuria
Xanthinuria, Type I
Xanthinuria, Type Ii
Xanthogranulomatous Pyelonephritis
X-Linked Diffuse Leiomyomatosis-Alport Syndrome |
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