Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Loss of vision
ID	http://purl.bioontology.org/ontology/OMIM/MTHU001331
cui	C3665346
Manifestation of	http://purl.bioontology.org/ontology/OMIM/300100 http://purl.bioontology.org/ontology/OMIM/500001 http://purl.bioontology.org/ontology/OMIM/203700 http://purl.bioontology.org/ontology/OMIM/300660 http://purl.bioontology.org/ontology/OMIM/301835 http://purl.bioontology.org/ontology/OMIM/609056 http://purl.bioontology.org/ontology/OMIM/176690 http://purl.bioontology.org/ontology/OMIM/222448 http://purl.bioontology.org/ontology/OMIM/254780
notation	MTHU001331
prefLabel	Loss of vision
tui	T184
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000020

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/SYMP_0000321	Human Disease Ontology 123	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50638	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/ICD10/H54.7	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10CM/H54.7	International Classification of Diseases, Version 10 - Clinical Modification	CUI