Disease #01690 (CDG2A (glycosylation, congenital disorder of, type IIa (CDG-2A)), OMIM:212066)

Official abbreviation CDG2A
Name glycosylation, congenital disorder of, type IIa (CDG-2A)
OMIM ID 212066
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MGAT2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00409547 K1278 PubMed: Oishi 2018 - M - Japan - - - - - CDG2A best corrected visual acuity: 0.6; electroretinogram , rod: mildly reduced, cone: severely reduced CYP4V2 CYP4V2 1 1 LOVD
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