Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	BEHCET SYNDROME
Synonyms	BD
ID	http://purl.bioontology.org/ontology/OMIM/109650
altLabel	BD BEHCET DISEASE
cui	C0004943
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	109650
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	BEHCET SYNDROME
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34416	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0004943	MedlinePlus Health Topics	CUI
http://purl.bmicc.cn/ontology/ICD10CN/M35.2	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/M35.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D001528	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D001528	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/LNC/LA17787-5	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/ICD10/M35.2	International Classification of Diseases, Version 10	CUI