Gene: [10^/USH1F] Usher syndrome 1F (autosomal recessive, severe; retinitis/deafness);


PAT

 The Usher syndromes are a group of autosomal recessive disorders characterized by progressive pigmentary retinopathy and sensorineural hearing loss, see details in: GEM:14q32/USH1A."

REF

 PAT,LOC,LIN "Wayne S &: AJHG, 61, (Suppl), A300, 1997

KEY

 eye, neu

CLA

 unknown, basic

LOC

 10

MIM

 MIM: 602083