MeSH Browser

MeSH Supplementary: Usher syndrome, type 1B
Unique ID: C536485
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536485
Registry Numbers: 0
Heading Mapped to: *Usher Syndromes
Frequency: 12
Note: A form of Usher Syndrome Type I characterized by severe hearing loss due to vestibular dysfunction. It is caused by mutations in the myosin VIIa (MYO7A) gene. OMIM: 276900
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Usher syndrome, type 1B MeSH Supplementary Concept Data 2025