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ENCongenital Disorder of Glycosylation, Type Iiw (CDG2W)
Alias:
Cdg2w
Congenital Disorder of Glycosylation 2w
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Congenital Disorder of Glycosylation, Type Iiw, is also known as cdg2w. An important gene associated with Congenital Disorder of Glycosylation, Type Iiw is SLC37A4 (Solute Carrier Family 37 Member 4). Affiliated tissues include liver, and related phenotypes are failure to thrive and hypotonia
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MALACARDS
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