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Diseases
Genes (1724)
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TBX5
Heart Arrhythmia
Holt–oram Syndrome
SLC6A19
Hartnup Disease
PYGM
Glycogen Storage Disease Type V
FECH
Erythropoietic Protoporphyria
PRPS1
Arts Syndrome
IFIH1
Singleton Merten Syndrome
Chronic Periodontitis
ACE
Heart Arrhythmia
Chronic Periodontitis
Glycogen Storage Disease Type V
ATXN3
Machado–joseph Disease
SLCO1B1
Hyperbilirubinemia, Rotor Type
NPM1
Acute Promyelocytic Leukemia
RARA
Acute Promyelocytic Leukemia
GJA1
Heart Arrhythmia
PRKAR1A
Fibrous Dysplasia Of Bone
Acute Promyelocytic Leukemia
Open Bite Malocclusion
NUMA1
Acute Promyelocytic Leukemia
SLCO1B3
Hyperbilirubinemia, Rotor Type
PML
Acute Promyelocytic Leukemia
Heart Arrhythmia
ZBTB16
Acute Promyelocytic Leukemia
TNF
Myocardial Stunning
Machado–joseph Disease
Acute Promyelocytic Leukemia
Heart Arrhythmia
Synovial Chondromatosis
Chronic Periodontitis
STAT5B
Acute Promyelocytic Leukemia
AKT1
Acute Promyelocytic Leukemia
Heart Arrhythmia
Corneal Neovascularization
Sirenomelia
Thrombophlebitis
Glycogen Storage Disease Type V