Any Usher syndrome in which the cause of the disease is a mutation in the WHRN gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: Usher syndrome caused by mutation in WHRN Usher syndrome type 2D USH2D Usher syndrome type IID WHRN Usher syndrome
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:15514 (OMIM:611383)
- OMIM:611383 (MONDO:equivalentTo)
- ICD10CM:H35.5 (MONDO:relatedTo)
- DOID:0110840 (MONDO:equivalentTo)
Subsets
gard_rare, rare, nord_rare, clingen