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Diseases
Genes (1269)
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TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
ATP7B
Wilson's Disease
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
Acute Promyelocytic Leukemia
RET
Acute Promyelocytic Leukemia
Potter Sequence
RARA
Acute Promyelocytic Leukemia
Potter Sequence
UBE3B
Kaufman Oculocerebrofacial Syndrome
TNF
Acute Promyelocytic Leukemia
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
Wilson's Disease
NPM1
Acute Promyelocytic Leukemia
IFIH1
Singleton Merten Syndrome
PRKAR1A
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
Pleural Effusion
ACTG2
Berdon Syndrome
NUMA1
Acute Promyelocytic Leukemia
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia