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Diseases
Genes (1441)
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TTPA
Familial Isolated Vitamin E Deficiency
ITGB3
Glanzmann's Thrombasthenia
PQBP1
Renpenning's Syndrome
ITGA2B
Glanzmann's Thrombasthenia
Thalassemia
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
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
ACTG2
Berdon Syndrome
PRKAR1A
Fibrous Dysplasia Of Bone
Acute Promyelocytic Leukemia
Enamel-Renal Syndrome
NUMA1
Acute Promyelocytic Leukemia
TP53
Occupational Cancer
Acute Promyelocytic Leukemia
Adenoid Cystic Carcinoma
PML
Acute Promyelocytic Leukemia
ZBTB16
Acute Promyelocytic Leukemia
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
SMC1A
Acute Promyelocytic Leukemia
Adenoid Cystic Carcinoma