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Diseases
Genes (4238)
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SCN5A
Progressive Familial Heart Block, Type Ib
Bundle Branch Block
Cardiomyopathy, Dilated, 1i
Atrial Fibrillation, Familial, 7
Atrial Standstill 1
NKX2-5
Progressive Familial Heart Block, Type Ib
Bundle Branch Block
Holt–oram Syndrome
Atrial Septal Defect 7 With Or Without Atrioventricular Conduction Defects
Cardiomyopathy, Dilated, 1i
Atrial Fibrillation, Familial, 7
ABCC9
Cardiomyopathy, Dilated, 1i
Cantú Syndrome
Atrial Fibrillation, Familial, 7
TP53
Occupational Cancer
Acute Promyelocytic Leukemia
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
Visual Impairment
ASL
Argininosuccinic Aciduria
Glioma Susceptibility 7
IDH1
Acute Promyelocytic Leukemia
Glioma Susceptibility 7
TNF
Acute Promyelocytic Leukemia
Neonatal Lupus Erythematosus
Agenesis
Myocardial Stunning
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
Systemic Inflammatory Response Syndrome
TBX5
Holt–oram Syndrome
SLC6A19
Hartnup Disease
PMM2
Pmm2 Deficiency
TTN
Cardiomyopathy, Dilated, 1i
Atrial Fibrillation, Familial, 7
TNFAIP3
Haploinsufficiency Of A20
Systemic Inflammatory Response Syndrome
PRPS1
Visual Impairment
Arts Syndrome
FGF2
Vascular Malformation
Corneal Neovascularization
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
RAF1
Acute Promyelocytic Leukemia
Bundle Branch Block
Cardiomyopathy, Dilated, 1i
Glioma Susceptibility 7
PTGS2
Acute Promyelocytic Leukemia
Arthrofibrosis
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
IFIH1
Singleton Merten Syndrome
Aortic Aneurysm, Familial Abdominal, 3
MMP9
Acute Promyelocytic Leukemia
Corneal Neovascularization
Agenesis
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
PTEN
Acute Promyelocytic Leukemia
Vascular Malformation
Aortic Aneurysm, Familial Abdominal, 3
Glioma Susceptibility 7
Systemic Inflammatory Response Syndrome
NPM1
Acute Promyelocytic Leukemia
Glioma Susceptibility 7