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Usher syndrome type I
Clinical manifestations:
- profound congenital sensorineural deafness
- absent vestibular function
- prepubertal onset of progressive retinitis pigmentosa leading
- more severe than types 2 or 3
Specific
Usher syndrome type 1B/myosin VIIA mutation associated
Usher syndrome type IA
Usher syndrome type IC/chromosome 11p associated (Usher syndrome type 1 Acadian variety)
Usher syndrome type ID
Usher syndrome type ID/F
Usher syndrome type IE
Usher syndrome type IF
Usher syndrome type IG
General
Usher syndrome
Database Correlations
OMIM correlations
MORBIDMAP 276903