Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Colorblindness
ID	http://purl.bioontology.org/ontology/OMIM/MTHU023012
cui	C0242225
Manifestation of	http://purl.bioontology.org/ontology/OMIM/262300
notation	MTHU023012
prefLabel	Colorblindness
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000020

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0242225	MedlinePlus Health Topics	CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0242225	MedlinePlus Health Topics	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3891	National Cancer Institute Thesaurus	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/H53.5	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.5	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.obolibrary.org/obo/DOID_13399	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/D003117	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10CM/H53.50	International Classification of Diseases, Version 10 - Clinical Modification	CUI