Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

CYTOCHROME c OXIDASE ASSEMBLY FACTOR COX10

Synonyms

HEME A:FARNESYLTRANSFERASE

ID

http://purl.bioontology.org/ontology/OMIM/602125

altLabel

HEME A:FARNESYLTRANSFERASE

COX10

COX10, S. CEREVISIAE, HOMOLOG OF

MITOCHONDRIAL COMPLEX IV DEFICIENCY

LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY

cui

C0268237

C1850599

C1413629

Gene Locus

17p12-p11.2

Gene Symbol

COX10

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/602125.0003

http://purl.bioontology.org/ontology/OMIM/602125.0004

http://purl.bioontology.org/ontology/OMIM/602125.0005

http://purl.bioontology.org/ontology/OMIM/602125.0001

http://purl.bioontology.org/ontology/OMIM/602125.0002

http://purl.bioontology.org/ontology/OMIM/602125.0006

MIMTYPEMEANING

Gene with known sequence

notation

602125

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

CYTOCHROME c OXIDASE ASSEMBLY FACTOR COX10

tui

T028

T019

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C564963 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/LNC/LP36619-2 Logical Observation Identifier Names and Codes CUI
http://purl.bioontology.org/ontology/MESH/D030401 Medical Subject Headings CUI