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combined oxidative phosphorylation deficiency (MONDO:0000732) definit… #8407

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combined oxidative phosphorylation deficiency (MONDO:0000732) definit… #8407

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3 changes: 2 additions & 1 deletion src/ontology/mondo-edit.obo
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Expand Up @@ -9654,7 +9654,7 @@ replaced_by: MONDO:0019347
[Term]
id: MONDO:0000732
name: combined oxidative phosphorylation deficiency
def: "A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes." [https://orcid.org/0000-0002-6601-2165]
def: "A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes are affected." [https://orcid.org/0000-0002-5002-8648, https://orcid.org/0000-0002-6601-2165]
subset: gard_rare {source="MONDO:GARD"}
subset: nord_rare {source="MONDO:NORD"}
subset: otar {source="MONDO:OTAR"}
Expand All @@ -9666,6 +9666,7 @@ xref: OMIMPS:609060 {source="MONDO:equivalentTo", source="https://orcid.org/0000
xref: UMLS:C4540031 {source="MEDGEN:1626645", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
is_a: MONDO:0016387 {source="https://orcid.org/0000-0002-6601-2165"} ! mitochondrial oxidative phosphorylation disorder
relationship: has_characteristic MONDO:0021152 {source="OMIMPS:609060"} ! inherited
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8216" xsd:anyURI
property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/12893/combined-oxidative-phosphorylation-deficiency" xsd:anyURI {source="GARD:0012893"}

[Term]
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