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Diseases
Genes (1088)
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NEXN
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Dilated, 1y
ELP1
Familial Dysautonomia
CDKN1C
Beckwith-Wiedemann Syndrome
SCN5A
Arrhythmogenic Cardiomyopathy
Cardiomyopathy, Dilated, 1y
ADA2
Sneddon Syndrome
MMP9
Aneurysm
Abdominal Aortic Aneurysm
Febrile Neutrophilic Dermatosis
TTN
Arrhythmogenic Cardiomyopathy
Cardiomyopathy, Dilated, 1y
COL3A1
Aneurysm
Abdominal Aortic Aneurysm
Uterine Rupture
Cystocele
IGF2
Beckwith-Wiedemann Syndrome
H19
Beckwith-Wiedemann Syndrome
KCNQ1OT1
Beckwith-Wiedemann Syndrome
PLD1
Cardiac Valvular Defect, Developmental
HLA-DRB1
Leptospirosis
Abdominal Aortic Aneurysm
Primary Membranous Glomerulonephritis
Giant Cell Arteritis
SOD2
Abdominal Aortic Aneurysm
Primary Membranous Glomerulonephritis
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
MMP14
Abdominal Aortic Aneurysm
CD55
Protein Losing Enteropathy
KCNQ1
Beckwith-Wiedemann Syndrome
Arrhythmogenic Cardiomyopathy
PKP2
Arrhythmogenic Cardiomyopathy
DSG2
Arrhythmogenic Cardiomyopathy
Cardiomyopathy, Dilated, 1y