Autosomal Dominant Myosin Storage Congenital Myopathy 7A

Preferred Label : Autosomal Dominant Myosin Storage Congenital Myopathy 7A;

NCIt synonyms : CMYP7A;

NCIt definition : An autosomal dominant form of congenital myopathy caused by mutation(s) in the MYH7 gene, encoding myosin-7.;

Details

Origin ID

C206090;

Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]

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