Term Name: autosomal dominant limb-girdle muscular dystrophy type 2
Synonyms: autosomal dominant limb-girdle muscular dystrophy type 1F, LGMD1F, muscular dystrophy limb-girdle type 1F
Definition: An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the TNPO3 gene on chromosome 7q32.
Ontology: Human Disease [DOID:0110304]   ( DOID:0110304 )

Relationships
is a type of: autosomal dominant limb-girdle muscular dystrophy