Ontology of Genes and Genomes

Last uploaded: February 21, 2019

Preferred Name	COMA
ID	http://purl.obolibrary.org/obo/OGG_3000266710
description	Cogan-type congential oculomotor apraxia
chromosome ID of gene	2
definition source	WEB: http://www.ncbi.nlm.nih.gov/gene
gene map location	2q13
label	COMA
modification date	20140305
NCBI GeneID	266710
nomenclature status	NCBI-supplied
organism NCBITaxon ID	9606
prefixIRI	OGG:3000266710
prefLabel	COMA
term editor	Bin Zhao, Yue Liu, Oliver He
subClassOf	http://purl.obolibrary.org/obo/OGG_2260009606

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/SYMP_0000605	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/ICD10CM/R40.2	International Classification of Diseases, Version 10 - Clinical Modification	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34497	National Cancer Institute Thesaurus	LOOM
http://purl.obolibrary.org/obo/HP_0001259	International Classification of Diseases Ontology	LOOM
http://purl.bioontology.org/ontology/MESH/D003128	Medical Subject Headings	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/MB20.1	International Classification of Diseases, 11th Edition, China	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU002540	Online Mendelian Inheritance in Man	LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0009421	MedlinePlus Health Topics	LOOM
http://www.semanticweb.org/ontologies/2009/3/ontoDPN.owl#Coma	Early Pregnancy Ontology	LOOM