Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	CYTOCHROME c OXIDASE ASSEMBLY FACTOR COX15
Synonyms	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2
ID	http://purl.bioontology.org/ontology/OMIM/603646
altLabel	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2 COX15 COX15, S. CEREVISIAE, HOMOLOG OF LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY
cui	C3554534 C1413632 C1850599
Gene Locus	10q24
Gene Symbol	COX15 CEMCOX2
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/603646.0002 http://purl.bioontology.org/ontology/OMIM/603646.0004 http://purl.bioontology.org/ontology/OMIM/603646.0003 http://purl.bioontology.org/ontology/OMIM/603646.0001
MIMTYPEMEANING	Gene with known sequence
notation	603646
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	CYTOCHROME c OXIDASE ASSEMBLY FACTOR COX15
tui	T028 T047

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C564963	Medical Subject Headings	CUI