All diseases

OMIM ID
612674
OMIM term:
POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT; PHARC
Alternative terms:

(∗) Location:
20p11.21  
(†) Associated OMIM genes:
ABHD12  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jhw1vwao