From e1958597982819c2a90e962c010354c04fb65aba Mon Sep 17 00:00:00 2001 From: katiermullen <102704401+katiermullen@users.noreply.github.com> Date: Fri, 15 Nov 2024 10:56:15 -0700 Subject: [PATCH] combined oxidative phosphorylation deficiency (MONDO:0000732) definition is truncated Closes #8216 --- src/ontology/mondo-edit.obo | 3 ++- 1 file changed, 2 insertions(+), 1 deletion(-) diff --git a/src/ontology/mondo-edit.obo b/src/ontology/mondo-edit.obo index 3a4d2bcd6..2b037a780 100644 --- a/src/ontology/mondo-edit.obo +++ b/src/ontology/mondo-edit.obo @@ -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"} @@ -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]