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Diseases
Genes (1479)
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ASL
Argininosuccinic Aciduria
HMBS
Acute Intermittent Porphyria
PMM2
Pmm2 Deficiency
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
TNFAIP3
Haploinsufficiency Of A20
IL1B
Ophthalmia
Merrf Syndrome
Membranoproliferative Glomerulonephritis
Cystinosis
Congenital Contractural Arachnodactyly
Renpenning's Syndrome
PQBP1
Renpenning's Syndrome
GALE
Galactose Epimerase Deficiency
LIPA
Acid Lipase Disease
Squamous-Cell Carcinoma Of The Lung
IFIH1
Singleton Merten Syndrome
TRNL1
Merrf Syndrome
FGFR2
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
EGFR
Primary Peritoneal Carcinoma
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Squamous-Cell Carcinoma Of The Lung
CFH
Membranoproliferative Glomerulonephritis
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
BRCA1
Primary Peritoneal Carcinoma