All diseases

OMIM ID
300580
OMIM term:
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX
Alternative terms:

(∗) Location:
Xq13.1-q22.1  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/mhf8egh6