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Diseases
Genes (1745)
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TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
TNF
Liver Failure
Acute Liver Failure
Thalassemia
Acute Promyelocytic Leukemia
Chronic Periodontitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Adenoid Cystic Carcinoma
PQBP1
Renpenning's Syndrome
ITGA2B
Thalassemia
Glanzmann's Thrombasthenia
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ASS1
Liver Failure
Citrullinemia Type I
UBE3B
Kaufman Oculocerebrofacial Syndrome
BCOR
Acute Promyelocytic Leukemia
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
Chronic Periodontitis
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
TP53
Occupational Cancer
Liver Failure
Acute Liver Failure
Acute Promyelocytic Leukemia
Adenoid Cystic Carcinoma
ACTG2
Berdon Syndrome
PRKAR1A
Fibrous Dysplasia Of Bone
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
NUMA1
Acute Promyelocytic Leukemia
ATP7B
Liver Failure
Acute Liver Failure
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia