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Metadata
ID DOID:0070260
Name congenital disorder of glycosylation type IIh
Definition A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG8 gene on chromosome 16q22.1.
https://www.ncbi.nlm.nih.gov/pubmed/17220172
Xrefs

GARD:12411

MESH:C566987

MIM:611182

ORDO:95428

SNOMEDCT_US_2023_03_01:717774004

UMLS_CUI:C1970021

Subsets

DO_rare_slim

Synonyms

Carbohydrate deficient glycoprotein syndrome type IIh [EXACT]

CDG IIh [EXACT]

CDG2H [EXACT]

CDGIIh [EXACT]

COG8-CDG [EXACT]

Congenital disorder of glycosylation type 2h [EXACT]

Parent Relationships

is_a autosomal recessive disease

is_a congenital disorder of glycosylation type II

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