Term Name: distal myopathy 1
Synonyms: Distal myopathy type 1, Gowers disease, Laing distal myopathy, Laing early-onset distal myopathy, MPD1
Definition: A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2.
Ontology: Human Disease [DOID:0070197]   ( DOID:0070197 )

Relationships
is a type of: autosomal dominant disease distal myopathy