PGM1-congenital disorder of glycosylation

Findings

No curated finding names PGM1-congenital disorder of glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Autosomal recessive inheritance

HPO, annotations 2026-09-02

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• congenital disorder of glycosylation type I
• disorder of protein N-glycosylation
• familial dilated cardiomyopathy

Resolves to: PGM1-congenital disorder of glycosylation

Also called

CDG syndrome type ItCDG-ItCDG1Tcongenital disorder of glycosylation type 1tcongenital disorder of glycosylation type ItPGM1-CDGphosphoglucomutase-1 deficiency