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1 Familial dilated cardiomyopathy Description Fami...
1 CHARGE syndrome Description CHARGE syndrome is a...
1 Leukoencephalopathy with vanishing white matter ...
1 ANTXR2 gene ANTXR cell adhesion molecule 2 Norma...
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1 Cystic fibrosis Description Cystic fibrosis is a...
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1 Multiple system atrophy Description Multiple sys...
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1 Atopic dermatitis Description also known as atop...
1 Dermatofibrosarcoma protuberans Description Derm...
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1 EGFR gene epidermal growth factor receptor Norma...
1 ADAMTS2 gene ADAM metallopeptidase with thrombos...
1 Ellis-van Creveld syndrome Description Ellis-van...
1 Childhood absence epilepsy Description epilepsye...
1 Essential tremor Description Essential tremor is...
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1 Factor X deficiency Description Factor X deficie...
1 FBLN5 gene fibulin 5 Normal Function The FBLN5 ...
1 Sandhoff disease Description Sandhoff disease is...
1 Pantothenate kinase-associated neurodegeneration...
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1 Hereditary angioedema Description Hereditary ang...
1 Horner syndrome Description Horner syndrome is a...
1 Hypertension Description Hypertension is abnorma...
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