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Diseases
Genes (1746)
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PMM2
Pmm2 Deficiency
Hyperinsulinism
ASL
Argininosuccinic Aciduria
ABCD1
Adrenoleukodystrophy
TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
RET
Acute Promyelocytic Leukemia
Pheochromocytoma
TNF
Adrenoleukodystrophy
Acute Promyelocytic Leukemia
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Morphea
Pheochromocytoma
KCNC3
Spinocerebellar Ataxia Type-13
PQBP1
Renpenning's Syndrome
SDHD
Acute Promyelocytic Leukemia
Pheochromocytoma
VHL
Acute Promyelocytic Leukemia
Pheochromocytoma
ITGA2B
Glanzmann's Thrombasthenia
MED12
Fg Syndrome
MAX
Pheochromocytoma
TMEM127
Pheochromocytoma
SDHB
Pheochromocytoma
FAM20A
Enamel-Renal Syndrome
PRKAR1A
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
Pheochromocytoma
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia