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DO Term : combined oxidative phosphorylation deficiency 28 [DOID:0111470] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A26 gene on chromosome 3p14.1.
  • synonyms:
  • COXPD28,
  • ORDO:466784,
  • neonatal severe cardiopulmonary failure due to mitochondrial methylation defect,
  • 616794,
  • OMIM:616794
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct parents





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