All diseases

OMIM ID
601419
OMIM term:
MYOPATHY, MYOFIBRILLAR, 1; MFM1
Alternative terms:
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
DESMINOPATHY, PRIMARY
DESMIN-RELATED MYOPATHY; DRM
INCLUSION BODY MYOPATHY 1, AUTOSOMAL DOMINANT, FORMERLY; IBM1, FORMERLY
CARDIOMYOPATHY, DILATED, 1F AND LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1D, FORMERLY
CMD1F AND LGMD1D, FORMERLY
CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT AND MUSCULAR DYSTROPHY; CDCD3, FORMERLY
(∗) Location:
2q35  
(†) Associated OMIM genes:
DES  
(‡) Associated MGI genes:
Des  

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