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Diseases
Genes (1385)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
SLC34A2
Pulmonary Alveolar Microlithiasis
PDGFRB
Acute Promyelocytic Leukemia
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
PRKAR1A
Acute Promyelocytic Leukemia
Fibrolamellar Hepatocellular Carcinoma
Congenital Contractural Arachnodactyly
Enamel-Renal Syndrome
NUMA1
Acute Promyelocytic Leukemia
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia
CFH
Membranoproliferative Glomerulonephritis
STAT5B
Acute Promyelocytic Leukemia
IRF2BP2
Acute Promyelocytic Leukemia