disorder of protein O-glycosylation
MONDO:0017741Mondo
Findings
No curated finding names disorder of protein O-glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A disease that has its basis in the disruption of protein O-linked glycosylation.
Definition from the Mondo Disease Ontology (MONDO:0017741), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (6)
- autosomal recessive limb-girdle muscular dystrophy type 2R1
- disorder of fucoglycosan synthesis
- myopathy caused by variation in FKRP
- myopathy caused by variation in POMGNT1
- myopathy caused by variation in POMGNT2
- qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan
Other names
2 names
Resolves to: disorder of protein O-glycosylation
- Also called
- disorder of protein O-linked glycosylationprotein O-linked glycosylation disease