All diseases

OMIM ID
255310
OMIM term:
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION; CFTD
Alternative terms:

(∗) Location:
1p36.11   1q21.3   1q42.13  
(†) Associated OMIM genes:
ACTA1   SEPN1   TPM3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1mm5ikqf