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Diseases
Genes (1064)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
GALE
Galactose Epimerase Deficiency
CFH
Membranoproliferative Glomerulonephritis
Pleural Effusion
IFIH1
Singleton Merten Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
PDGFB
Primary Familial Brain Calcification
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
YAP1
Epithelioid Hemangioendothelioma
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
WWTR1
Epithelioid Hemangioendothelioma
Congenital Contractural Arachnodactyly
TFE3
Epithelioid Hemangioendothelioma
Vascular Tumor
CAMTA1
Epithelioid Hemangioendothelioma