Myofibrillar Myopathy 3

Preferred Label : Myofibrillar Myopathy 3;

NCIt synonyms : MFM3;

NCIt definition : An autosomal dominant subtype of myofibrillar myopathy caused by mutation(s) in the MYOT gene, encoding myotilin.;

Details

Origin ID

C206517;

Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]

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