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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:combined oxidative phosphorylation deficiency 25
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Accession:DOID:0111468 term browser browse the term
Definition:A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in MARS2 on chromosome 2q33.1. (DO)
Synonyms:exact_synonym: COXPD25
 primary_id: OMIM:616430
 xref: EFO:0009035;   ORDO:447954
For additional species annotation, visit the Alliance of Genome Resources.

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combined oxidative phosphorylation deficiency 25 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mars2 methionyl-tRNA synthetase 2, mitochondrial ISO ClinVar Annotator: match by term: Combined oxidative phosphorylation deficiency 25 OMIM
PMID:25741868 PMID:25754315 NCBI chr 9:56,720,408...56,729,991
Ensembl chr 9:56,720,983...56,723,820
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18215
    Nutritional and Metabolic Diseases 6781
      disease of metabolism 6781
        mitochondrial metabolism disease 445
          combined oxidative phosphorylation deficiency 84
            combined oxidative phosphorylation deficiency 25 1
Path 2
Term Annotations click to browse term
  disease 18215
    Developmental Disease 13067
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11805
        genetic disease 11316
          monogenic disease 8884
            autosomal genetic disease 7927
              autosomal recessive disease 4933
                combined oxidative phosphorylation deficiency 25 1
paths to the root