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Metadata
ID	DOID:0050760
Name	X-linked myopathy with excessive autophagy
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. https://rarediseases.org/rare-diseases/x-linked-myopathy-with-excessive-autophagy/
Xrefs	GARD:3892 OMIM:310440
Subsets	DO_rare_slim
Synonyms	XMEA [EXACT]
Parent Relationships	is_a myopathy is_a X-linked recessive disease