Term Name:	X-linked myopathy with excessive autophagy
Synonyms:	XMEA
Definition:	A myopathy that is characterized by childhood onset of progressive muscle weakness and atrophy primarily affecting the proximal muscles in males between 5 and 10 years old, has_material_basis_in mutation in the VMA21 gene on chromosome Xq28.
Ontology:	Human Disease [DOID:0050760]   ( DOID:0050760 )