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mitochondrial complex IV deficiency nuclear type 11 - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:mitochondrial complex IV deficiency nuclear type 11
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Accession:DOID:0070497 term browser browse the term
Definition:A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX20 gene on chromosome 1q44. (DO)
Synonyms:exact_synonym: COX20-RELATED CONDITION;   MC4DN11
 primary_id: MIM:619054
 alt_id: DOID:9000374

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mitochondrial complex IV deficiency nuclear type 11 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cox20 cytochrome c oxidase assembly protein 20 ISO ClinVar Annotator: match by term: COX20-related condition | ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 11 OMIM
ClinVar		 PMID:9536098 PMID:17576681 PMID:23125284 PMID:24202787 PMID:25741868 More... NCBI chr 1:178,146,379...178,150,258
Ensembl chr 1:178,146,695...178,150,258 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16268
    Nutritional and Metabolic Diseases 7706
      disease of metabolism 7706
        mitochondrial metabolism disease 854
          cytochrome-c oxidase deficiency disease 250
            COX deficiency, benign infantile mitochondrial myopathy 48
              mitochondrial complex IV deficiency nuclear type 11 1
Path 2
Term Annotations click to browse term
  disease 16268
    Developmental Disease 14084
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13142
        genetic disease 12835
          inherited metabolic disorder 6082
            mitochondrial metabolism disease 854
              cytochrome-c oxidase deficiency disease 250
                COX deficiency, benign infantile mitochondrial myopathy 48
                  mitochondrial complex IV deficiency nuclear type 11 1
paths to the root