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Congenital disorder of glycosylation with deafness as a major feature

MedGen UID:: 1842667
•Concept ID:: C5680021
•: Disease or Syndrome

Synonyms:	CDG with deafness as a major feature; CDG with hearing loss as a major feature; Congenital disorder of glycosylation with hearing loss as a major feature

Orphanet:	ORPHA371212

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MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVCongenital disorder of glycosylation with deafness as a major feature

Congenital disorder of glycosylation with deafness as a major feature

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

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