Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	PILONIDAL SINUS
ID	http://purl.bioontology.org/ontology/OMIM/173000
cui	C0031925
MIMTYPEMEANING	Other, mainly phenotypes with suspected mendelian basis
notation	173000
OMIM Entry Type	0
OMIM MimType Value	none
prefLabel	PILONIDAL SINUS
tui	T190

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/L05.91	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10/L05	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0031925	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/ICD10CM/L05.92	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10CM/L05	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D010864	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D010864	Medical Subject Headings	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/L05	International Classification of Diseases, 10th Edition, China	CUI