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

More general terms

• Usher syndrome

More specific terms

• 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

Database

• OMIM: https://mirror.omim.org/entry/276900
• OMIM: https://mirror.omim.org/entry/276903
• OMIM: https://mirror.omim.org/entry/276904