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Diseases
Genes (1384)
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FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
PDGFRB
Acute Promyelocytic Leukemia
Primary Familial Brain Calcification
Congenital Contractural Arachnodactyly
SLC20A2
Primary Familial Brain Calcification
SLC34A2
Pulmonary Alveolar Microlithiasis
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
HSD17B3
True Hermaphroditism
Disorders Of Sex Development
GALE
Galactose Epimerase Deficiency
LHCGR
True Hermaphroditism
Disorders Of Sex Development
IFIH1
Singleton Merten Syndrome
AKR1C3
True Hermaphroditism
Disorders Of Sex Development
AKR1C1
True Hermaphroditism
Disorders Of Sex Development
AKR1C2
True Hermaphroditism
Disorders Of Sex Development
NUMA1
Acute Promyelocytic Leukemia
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia
CFH
Membranoproliferative Glomerulonephritis
STAT5B
Acute Promyelocytic Leukemia