All diseases

OMIM ID
304150
OMIM term:
OCCIPITAL HORN SYNDROME; OHS
Alternative terms:
CUTIS LAXA, X-LINKED, FORMERLY
EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY
EDS IX, FORMERLY
EDS9, FORMERLY
(∗) Location:
Xq21.1  
(†) Associated OMIM genes:
ATP7A  
(‡) Associated MGI genes:

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