Visualize Submit Comment
Metadata
ID DOID:0110826
Name Usher syndrome type 1
Definition An Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa.
https://ghr.nlm.nih.gov/condition/usher-syndrome, https://www.ncbi.nlm.nih.gov/books/NBK1265/, https://www.ncbi.nlm.nih.gov/pubmed/2909824
Xrefs

ICD10CM:H35.5

OMIM:276900

ORDO:231169

Subsets

DO_rare_slim

Synonyms

US1 [EXACT]

USH1 [EXACT]

Parent Relationships

is_a Usher syndrome

Add an item to the term tracker