FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term combined oxidative phosphorylation deficiency 55 ID (Ontology) DOID:0070428 (Human Disease)
Definition A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the POLRMT gene on chromosome 19p13.
Also Known As "COXPD55"
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 Genes
 combined oxidative phosphorylation deficiency 55       1
 for disease ribbon | combined oxidative phosphorylation deficiency 55       1
 model of | combined oxidative phosphorylation deficiency 55       1
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monogenic disease
 |__autosomal genetic disease______________________
mitochondrial metabolism disease                   |
 |__combined oxidative phosphorylation deficiency__|
                                                   combined oxidative phosphorylation deficiency 55  1 rec.
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Is a autosomal genetic disease
combined oxidative phosphorylation deficiency
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Synonyms
  • "COXPD55" EXACT OMO:0003012
Secondary IDs
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MIM:619743