Preferred Name |
Hereditary Optic Atrophy |
ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34864 |
ALT_DEFINITION |
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER). |
code |
C34864 |
label |
Hereditary Optic Atrophy |
Legacy_Concept_Name |
Hereditary_Optic_Atrophy |
Preferred_Name |
Hereditary Optic Atrophy |
prefixIRI |
C34864 |
prefLabel |
Hereditary Optic Atrophy |
Semantic_Type |
Disease or Syndrome Congenital Abnormality |
UMLS_CUI |
C0029125 |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/ICD10CM/H47.22 | International Classification of Diseases, Version 10 - Clinical Modification | LOOM |