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Diseases
Genes (1171)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
ATP7B
Wilson's Disease
SLC12A6
Andermann Syndrome
NGLY1
Ngly1 Deficiency
Corneal Neovascularization
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
MED12
Fg Syndrome
SLC17A5
Wilson's Disease
Salla Disease
FAM20A
Enamel-Renal Syndrome
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
NUMA1
Acute Promyelocytic Leukemia
ACTG2
Berdon Syndrome
PRKAR1A
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
ZBTB16
Acute Promyelocytic Leukemia
Salla Disease