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Diseases
Genes (1002)
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AVP
Diabetes Insipidus
Nephrogenic Diabetes Insipidus
Central Diabetes Insipidus
AVPR2
Diabetes Insipidus
Nephrogenic Diabetes Insipidus
Central Diabetes Insipidus
AQP2
Diabetes Insipidus
Nephrogenic Diabetes Insipidus
Central Diabetes Insipidus
FBN2
Congenital Contractural Arachnodactyly
Central Diabetes Insipidus
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
UMOD
Medullary Cystic Kidney Disease
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
SLC4A4
Nephrogenic Diabetes Insipidus
Proximal Renal Tubular Acidosis
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
CFH
Membranoproliferative Glomerulonephritis
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly