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 |
