All diseases

OMIM ID
601414
OMIM term:
RETINITIS PIGMENTOSA 18; RP18
Alternative terms:

(∗) Location:
1q21.2-q21.3  
(†) Associated OMIM genes:
PRPF3  
(‡) Associated MGI genes:
Prpf3  

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* quick link - http://q.sanger.ac.uk/zvud36n9