Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Optic nerve atrophy
ID	http://purl.bioontology.org/ontology/OMIM/MTHU036648
cui	C0029124
Manifestation of	http://purl.bioontology.org/ontology/OMIM/610708 http://purl.bioontology.org/ontology/OMIM/261680 http://purl.bioontology.org/ontology/OMIM/122860 http://purl.bioontology.org/ontology/OMIM/606056 http://purl.bioontology.org/ontology/OMIM/608553 http://purl.bioontology.org/ontology/OMIM/615085 http://purl.bioontology.org/ontology/OMIM/615597 http://purl.bioontology.org/ontology/OMIM/253280 http://purl.bioontology.org/ontology/OMIM/614225 http://purl.bioontology.org/ontology/OMIM/614222
notation	MTHU036648
prefLabel	Optic nerve atrophy
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000020

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Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/H47.2	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/H47.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D009896	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10CM/H47.20	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10/H47.2	International Classification of Diseases, Version 10	CUI