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Preferred Name

Hereditary Optic Atrophy
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34864
code

C34864
Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258
Contributing_Source

Cellosaurus
DEFINITION

A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
FULL_SYN

Hereditary Optic Atrophy
label

Hereditary Optic Atrophy
Legacy Concept Name

Hereditary_Optic_Atrophy
Preferred_Name

Hereditary Optic Atrophy
prefixIRI

Thesaurus:C34864
prefLabel

Hereditary Optic Atrophy
Semantic_Type

Disease or Syndrome

Congenital Abnormality
UMLS_CUI

C0029125
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34863
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0043878 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0043878 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/H47.22 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 LOOM