Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

MOTION SICKNESS
ID

http://purl.bioontology.org/ontology/OMIM/158280
cui

C0026603
MIMTYPEMEANING

Other, mainly phenotypes with suspected mendelian basis
notation

158280
OMIM Entry Type

0
OMIM MimType Value

none
prefLabel

MOTION SICKNESS
tui

T047
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http://purl.bioontology.org/ontology/MESH/D009041 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D009041 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026603 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0026603 MedlinePlus Health Topics LOOM
http://purl.obolibrary.org/obo/DOID_2951 Human Disease Ontology 123 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/NF08.3 International Classification of Diseases, 11th Edition, China LOOM
http://purl.bmicc.cn/ontology/ICD10CN/T75.3 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/ICD10CM/T75.3 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10CM/T75.3 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34824 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/ICD10/T75.3 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10/T75.3 International Classification of Diseases, Version 10 LOOM