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Preferred Name

Optic Atrophy
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34863
code

C34863
DEFINITION

A disorder characterized by loss of optic nerve fibers. It may be inherited or acquired. Acquired causes include ischemia, optic nerve neuropathy, glaucoma, trauma, radiation, brain tumors, and multiple sclerosis. It leads to vision disturbances.
FULL_SYN

Optic Atrophy
label

Optic Atrophy
Legacy Concept Name

Optic_Atrophy
Preferred_Name

Optic Atrophy
prefixIRI

Thesaurus:C34863
prefLabel

Optic Atrophy
Semantic_Type

Disease or Syndrome
UMLS_CUI

C3278618
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27604
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http://purl.bioontology.org/ontology/OMIM/MTHU036360 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0000648 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/H47.2 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/MESH/D009896 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/MONDO_0003608 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0003608 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/9C40.B 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/ICD10/H47.2 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.obolibrary.org/obo/DOID_5723 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_5723 Human Disease Ontology / 人类疾病本体 LOOM