Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	MENIERE DISEASE
ID	http://purl.bioontology.org/ontology/OMIM/156000
cui	C0025281
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU045194 http://purl.bioontology.org/ontology/OMIM/MTHU015056 http://purl.bioontology.org/ontology/OMIM/MTHU001112 http://purl.bioontology.org/ontology/OMIM/MTHU045195 http://purl.bioontology.org/ontology/OMIM/MTHU045193 http://purl.bioontology.org/ontology/OMIM/MTHU022612 http://purl.bioontology.org/ontology/OMIM/MTHU003968
MIMTYPEMEANING	Other, mainly phenotypes with suspected mendelian basis
notation	156000
OMIM Entry Type	0
OMIM MimType Value	none
prefLabel	MENIERE DISEASE
tui	T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/H81.0	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10/H81.0	International Classification of Diseases, Version 10	CUI
http://purl.bmicc.cn/ontology/ICD11CN/AB31.0	International Classification of Diseases, 11th Edition, China	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/H81.0	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/H81.09	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D008575	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D008575	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0025281	MedlinePlus Health Topics	CUI