Usher syndrome, type 1D/F
MONDO:0100050Mondo
Findings
No curated finding names Usher syndrome, type 1D/F yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any Usher syndrome in which the cause of the disease is a mutation in the CDH23 and PCDH15 genes.
Definition from the Mondo Disease Ontology (MONDO:0100050), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: Usher syndrome, type 1D/F
- Also called
- Usher syndrome, type 1D/F, CDH23/PCDH15, digenic