All diseases

OMIM ID
314580
OMIM term:
WIEACKER SYNDROME
Alternative terms:
CONTRACTURES OF FEET, MUSCLE ATROPHY, AND OCULOMOTOR APRAXIA
APRAXIA, OCULOMOTOR, WITH CONGENITAL CONTRACTURES AND MUSCLE ATROPHY
WIEACKER-WOLFF SYNDROME
(∗) Location:
Xq13-q21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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