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Diseases
Genes (1404)
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ASL
Argininosuccinic Aciduria
TBX5
Holt–oram Syndrome
PMM2
Pmm2 Deficiency
SLC6A19
Hartnup Disease
TNF
Acute Promyelocytic Leukemia
Asystole
Ophthalmia
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Tetraplegia
PYGM
Glycogen Storage Disease Type V
TTPA
Familial Isolated Vitamin E Deficiency
SGCE
Myoclonic Dystonia
IFNG
Acute Promyelocytic Leukemia
Asystole
Ophthalmia
Vascular Tumor
PRPS1
Arts Syndrome
Tetraplegia
PQBP1
Renpenning's Syndrome
LIPA
Acid Lipase Disease
Asystole
IFIH1
Singleton Merten Syndrome
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
TRNL1
Merrf Syndrome
VEGFA
Corneal Neovascularization
Acute Promyelocytic Leukemia
Asystole
Ophthalmia
Primary Peritoneal Carcinoma
Vascular Malformation
IL1B
Corneal Neovascularization
Merrf Syndrome
Acute Promyelocytic Leukemia
Asystole
Ophthalmia
Renpenning's Syndrome
ITGB2
Acute Promyelocytic Leukemia
Leukocyte Adhesion Deficiency, Type I
NUMA1
Acute Promyelocytic Leukemia