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Diseases
Genes (690)
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ASL
Argininosuccinic Aciduria
MYO5B
Microvillus Inclusion Disease
ATP7B
Wilson's Disease
POLG
Balo Concentric Sclerosis
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
TSLP
Membranoproliferative Glomerulonephritis
Lumbar Disc Disease
RAB27A
Hemophagocytic Lymphohistiocytosis
Platelet Storage Pool Deficiency
ANXA5
Wilson's Disease
PSTPIP1
Pyoderma Gangrenosum
RB1
Pinealoblastoma
Wilson's Disease
Hemangioendothelioma
Trilateral Retinoblastoma
XIAP
Hemophagocytic Lymphohistiocytosis
Wilson's Disease
GFI1B
Platelet Storage Pool Deficiency
TNF
Hemophagocytic Lymphohistiocytosis
Wilson's Disease
Lumbar Disc Disease
Pyoderma Gangrenosum
PRKACA
Fibrolamellar Hepatocellular Carcinoma