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Congenital disorder of glycosylation with epilepsy as a major feature

MedGen UID:: 1842998
•Concept ID:: C5679904
•: Disease or Syndrome

Synonym:	CDG with epilepsy as a major feature

Orphanet:	ORPHA371071

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MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVCongenital disorder of glycosylation with epilepsy as a major feature

Congenital disorder of glycosylation with epilepsy as a major feature

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Congenital disorder of glycosylation with epilepsy as a major feature
Congenital disorder of glycosylation with epilepsy as a major feature

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