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DO Term : combined oxidative phosphorylation deficiency [DOID:0060286] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A mitochondrial metabolism disease that is characterized by growth retardation, microcephaly, hypertonia, encephalopathy, cardiomyopathy and liver dysfunction.
  • synonyms:
  • PS609060,
  • GARD:12893,
  • OMIM:PS609060
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Disease

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Diseases --> Mouse models

Ontology

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