Usher syndrome type IA

Genetics

• associated with defects in JAG2

Clinical manifestations

• congenital sensory deafness associated with retinitis pigmentosa & feeble-mindedness
• also see Usher syndrome type I

More general terms

• Usher syndrome type I

Database

• OMIM: https://mirror.omim.org/entry/276900
• Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=7393