XYLT1-congenital disorder of glycosylation

Findings

No curated finding names XYLT1-congenital disorder of glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

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
• developmental anomaly of metabolic origin
• multiple congenital anomalies/dysmorphic syndrome-intellectual disability

Resolves to: XYLT1-congenital disorder of glycosylation

Also called

XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylationXYLT18-CDG