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Metadata
ID	DOID:0112110
Name	combined oxidative phosphorylation deficiency 49
Definition	A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MIEF2 gene on chromosome 17p11.2. https://pubmed.ncbi.nlm.nih.gov/29361167/
Xrefs	MIM:619024
Synonyms	COXPD49 [EXACT]
Parent Relationships	is_a combined oxidative phosphorylation deficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance