combined oxidative phosphorylation deficiency 19 Disease Ontology Browser

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combined oxidative phosphorylation deficiency 19 (DOID:0111476)
Alliance: disease page
Synonyms: COXPD19; severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
Alt IDs: OMIM:615595, ORDO:397593
Definition: A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the LYRM4 gene on chromosome 6p25.1.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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