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Diseases
Genes (1049)
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ASL
Argininosuccinic Aciduria
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
BRAF
Langerhans Cell Histiocytosis
Congenital Contractural Arachnodactyly
PQBP1
Renpenning's Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Hepatitis E
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis
Type Iii Hypersensitivity
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
IFNG
Hepatitis E
Cystinosis
Type Iii Hypersensitivity
Langerhans Cell Histiocytosis
Congenital Contractural Arachnodactyly
Cryptococcosis
Vascular Tumor
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
SOST
Craniodiaphyseal Dysplasia
Langerhans Cell Histiocytosis
ALB
Hepatitis E
Membranoproliferative Glomerulonephritis
Congenital Contractural Arachnodactyly
Disinhibition
DDX58
Hepatitis E
Singleton Merten Syndrome