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Diseases
Genes (979)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
BRAF
Langerhans Cell Histiocytosis
Congenital Contractural Arachnodactyly
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis
TNF
Listeriosis
Langerhans Cell Histiocytosis
Congenital Contractural Arachnodactyly
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Dysentery
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PRKACA
Fibrolamellar Hepatocellular Carcinoma
SOST
Craniodiaphyseal Dysplasia
Langerhans Cell Histiocytosis
ALB
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
Congenital Contractural Arachnodactyly
Disinhibition
DDX58
Singleton Merten Syndrome