Mondo Disease Ontology / Mondo疾病本体 - combined oxidative phosphorylation deficiency - Classes

Preferred Name	combined oxidative phosphorylation deficiency
Definitions	A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes.
ID	http://purl.obolibrary.org/obo/MONDO_0000732
database_cross_reference	OMIMPS:609060 GARD:0012893 DOID:0060286
definition	A mitochondrial oxidative phosphorylation disorder in which multiple mitochondrial respiratory chain complexes.
exactMatch	https://omim.org/phenotypicSeries/PS609060 http://purl.obolibrary.org/obo/DOID_0060286
id	MONDO:0000732
in_subset	http://purl.obolibrary.org/obo/mondo#gard_rare
label	combined oxidative phosphorylation deficiency
notation	MONDO:0000732
prefLabel	combined oxidative phosphorylation deficiency
seeAlso	https://rarediseases.info.nih.gov/diseases/12893/combined-oxidative-phosphorylation-deficiency
treeView	http://purl.obolibrary.org/obo/MONDO_0016387
subClassOf	http://purl.obolibrary.org/obo/MONDO_0016387

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/MTHU059541	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://purl.obolibrary.org/obo/MONDO_0000732	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0000732	Experimental Factor Ontology / 实验性因素本体	SAME_URI
http://purl.obolibrary.org/obo/DOID_0060286	Human Disease Ontology / 人类疾病本体	LOOM