All diseases

OMIM ID
600110
OMIM term:
STARGARDT DISEASE 3; STGD3
Alternative terms:
MACULAR DYSTROPHY WITH FLECKS, TYPE 3
STARGARDT-LIKE MACULAR DYSTROPHY, AUTOSOMAL DOMINANT
(∗) Location:
6q14.1  
(†) Associated OMIM genes:
ELOVL4  
(‡) Associated MGI genes:
Elovl4  

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* quick link - http://q.sanger.ac.uk/6r3j00p9