Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	RETINAL DETACHMENT
ID	http://purl.bioontology.org/ontology/OMIM/180050
cui	C0035305
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	180050
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	RETINAL DETACHMENT
tui	T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_5327	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0035305	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0035305	MedlinePlus Health Topics	LOOM
http://purl.bioontology.org/ontology/ICD10CM/H33.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D012163	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D012163	Medical Subject Headings	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26874	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/LNC/LA24876-7	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/LNC/LA24876-7	Logical Observation Identifier Names and Codes	LOOM
http://purl.bmicc.cn/ontology/HPCH/HP_0000541	Human Phenotype Ontology China	LOOM