Human genes for combined oxidative phosphorylation deficiency 9
Combined oxidative phosphorylation deficiency 9 [DOID:0111472]
A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in MRPL3 on chromosome 3q22.1.
Synonyms: combined oxidative phosphorylation deficiency 9, DOID:0111472, COXPD9