All diseases

OMIM ID
612095
OMIM term:
RETINITIS PIGMENTOSA 41; RP41
Alternative terms:

(∗) Location:
4p15.32  
(†) Associated OMIM genes:
PROM1  
(‡) Associated MGI genes:
Prom1  

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* quick link - http://q.sanger.ac.uk/fwmy4dsj