MeSH Treeview
Query OMIM entry list
610768
CDG1M
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im
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Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Database Center for Life Science
