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Diseases
Genes (1133)
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COL3A1
Aneurysm
Uterine Rupture
Ehlers-Danlos Syndrome, Vascular Type
Cystocele
Abdominal Aortic Aneurysm
MYH6
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 14
NEXN
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Dilated, 1y
LIPA
Lysosomal Acid Lipase Deficiency
SH2D1A
Lymphoproliferative Syndrome, X-Linked, 1
DICER1
Pleuropulmonary Blastoma
Pinealoblastoma
FXN
Friedreich Ataxia 1
PDGFB
Primary Familial Brain Calcification
Meningioma, Familial, Susceptibility To
CFH
Pleural Effusion
Complement Factor H Deficiency
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
SCO2
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency 2
Abdominal Aortic Aneurysm
IFNGR2
Immunodeficiency 28
FLNC
Cardiomyopathy, Dilated, 1y
Cardiomyopathy, Familial Hypertrophic, 26
ARV1
Epileptic Encephalopathy, Early Infantile, 38
TTN
Cardiomyopathy, Dilated, 1y
MMP9
Aneurysm
Cholesteatoma
Pleural Effusion
Abdominal Aortic Aneurysm
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