All diseases

OMIM ID
126600
OMIM term:
DOYNE HONEYCOMB RETINAL DYSTROPHY; DHRD
Alternative terms:
DOYNE HONEYCOMB DEGENERATION OF RETINA; DHD MALATTIA LEVENTINESE, INCLUDED; MLVT, INCLUDED
DRUSEN, RADIAL, AUTOSOMAL DOMINANT, INCLUDED
(∗) Location:
2p16.1  
(†) Associated OMIM genes:
EFEMP1  
(‡) Associated MGI genes:
Efemp1  

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