Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Raynaud phenomenon
ID	http://purl.bioontology.org/ontology/OMIM/MTHU025938
cui	C0034735
Manifestation of	http://purl.bioontology.org/ontology/OMIM/192315 http://purl.bioontology.org/ontology/OMIM/259900 http://purl.bioontology.org/ontology/OMIM/613471 http://purl.bioontology.org/ontology/OMIM/615688 http://purl.bioontology.org/ontology/OMIM/616260 http://purl.bioontology.org/ontology/OMIM/611773
notation	MTHU025938
prefLabel	Raynaud phenomenon
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000083 http://purl.bioontology.org/ontology/OMIM/MTHU000113 http://purl.bioontology.org/ontology/OMIM/MTHU000139

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/D011928	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10/I73.0	International Classification of Diseases, Version 10	CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50724	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0034735	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/ICD10CM/I73.0	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.obolibrary.org/obo/HP_0030880	Human Phenotype Ontology China	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/BD42	International Classification of Diseases, 11th Edition, China	LOOM