FAM20B-congenital disorder of glycosylation
MONDO:0100588Mondo
Findings
No curated finding names FAM20B-congenital disorder of glycosylation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any congenital disorder of glycosylation in which the cause of the disease is a mutation in FAM20B.
Definition from the Mondo Disease Ontology (MONDO:0100588), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: FAM20B-congenital disorder of glycosylation
- Also called
- FAM20B-CDG