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Diseases
Genes (802)
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MYH6
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 14
NEXN
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Dilated, 1y
LIPA
Lysosomal Acid Lipase Deficiency
PLN
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 18
SCO2
Abdominal Aortic Aneurysm
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
FLNC
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 26
MYL2
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 10
MMP9
Aneurysm
Abdominal Aortic Aneurysm
GYS1
Glycogen Storage Disease 0, Muscle
TTN
Cardiomyopathy, Dilated, 1y
PLD1
Cardiac Valvular Defect, Developmental
COA6
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
COL3A1
Aneurysm
Abdominal Aortic Aneurysm
Uterine Rupture
MMP14
Abdominal Aortic Aneurysm
SOD2
Abdominal Aortic Aneurysm
CD55
Protein Losing Enteropathy
DAB2IP
Abdominal Aortic Aneurysm
COX15
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
COA5
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2