Hereditary Optic Atrophy

Preferred Label : Hereditary Optic Atrophy;

NCIt 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.;

Details

Origin ID

C34864;

UMLS CUI

C0029125;

Automatic exact mappings (from CISMeF team)
- Hereditary optic atrophy [ICD-9 code]
Currated CISMeF NLP mapping
- Hereditary optic atrophy [MedDRA Preferred Term]
- Hereditary optic atrophy (disorder) [SNOMED CT concept]
- hereditary optic atrophy [Disease (Nov.)]
- hereditary optic atrophy, nos [SNOMED Notion]
- optic atrophies, hereditary [MeSH Descriptor]
- optic atrophies, hereditary [MeSH concept]
Has associated anatomic sites
- Eye [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary optic atrophy [ICD-9 code]
- Hereditary optic atrophy [MedDRA Preferred Term]
- Hereditary optic atrophy (disorder) [SNOMED CT concept]
- hereditary optic atrophy [Disease (Nov.)]
- hereditary optic atrophy, nos [SNOMED Notion]
- optic atrophies, hereditary [MeSH concept]
- optic atrophies, hereditary [MeSH Descriptor]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Hereditary Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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