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Diseases
Genes (784)
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MYH6
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 14
NEXN
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Dilated, 1y
ASL
Argininosuccinic Aciduria
LIPA
Lysosomal Acid Lipase Deficiency
PMM2
Pmm2 Deficiency
PLN
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 18
COL2A1
Collagen, Type Ii, Alpha-1
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
TTN
Cardiomyopathy, Dilated, 1y
PLD1
Cardiac Valvular Defect, Developmental
COA6
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
PAH
Phenylketonuria
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
COL3A1
Aneurysm
Abdominal Aortic Aneurysm
Uterine Rupture
MMP14
Abdominal Aortic Aneurysm
SOD2
Abdominal Aortic Aneurysm
COX15
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2