optic atrophies, hereditary

Preferred Label : optic atrophies, hereditary;

MeSH 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).;

MeSH synonym : optic atrophy, hereditary; hereditary optic atrophy; atrophies, hereditary optic; atrophy, hereditary optic; hereditary optic atrophies;

Wikipedia link : https://en.wikipedia.org/wiki/Optic atrophies, hereditary;

Details

Origin ID

D015418;

UMLS CUI

C0029125;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- Hereditary Optic Atrophy [NCIt concept]
- Hereditary optic atrophy [MedDRA Preferred Term]
- Hereditary optic atrophy (disorder) [SNOMED CT concept]
- hereditary optic atrophy [Disease (Nov.)]
- hereditary optic atrophy, nos [SNOMED Notion]
Record concept(s)
- optic atrophies, hereditary [MeSH concept]
Related MeSH Supplementary Concept(s)
- Berk-Tabatznik syndrome [MeSH Supplementary Concept]
- Senior-Loken syndrome 3 [MeSH Supplementary Concept]
- Senior-Loken syndrome 5 [MeSH Supplementary Concept]
- Senior-Loken syndrome 6 [MeSH Supplementary Concept]
- friedreich ataxia, So-Called, with optic atrophy and sensorineural deafness [MeSH Supplementary Concept]
- growth retardation, alopecia, pseudoanodontia and optic atrophy [MeSH Supplementary Concept]
- hagemoser weinstein bresnick syndrome [MeSH Supplementary Concept]
- konigsmark knox hussels syndrome [MeSH Supplementary Concept]
- metaphyseal dysplasia, anetoderma, and optic atrophy [MeSH Supplementary Concept]
- necrotizing encephalomyelopathy, subacute, of leigh, adult [MeSH Supplementary Concept]
- optic atrophy 1 and deafness [MeSH Supplementary Concept]
- optic atrophy 4 [MeSH Supplementary Concept]
- optic atrophy 5 [MeSH Supplementary Concept]
- optic atrophy 6 [MeSH Supplementary Concept]
- optic atrophy 7 [MeSH Supplementary Concept]
- optic atrophy and cataract, autosomal dominant [MeSH Supplementary Concept]
- optic atrophy polyneuropathy deafness [MeSH Supplementary Concept]
- optic atrophy spastic paraplegia syndrome [MeSH Supplementary Concept]
- optic atrophy with demyelinating disease of CNS [MeSH Supplementary Concept]
- optic atrophy with negative electroretinograms [MeSH Supplementary Concept]
- optic atrophy, deafness, ophthalmoplegia, and myopathy [MeSH Supplementary Concept]
- senior loken syndrome [MeSH Supplementary Concept]
- spastic paraplegia, optic atrophy, and dementia [MeSH Supplementary Concept]
- spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal [MeSH Supplementary Concept]
- wolfram syndrome, mitochondrial form [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- optic atrophy [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary Optic Atrophy [NCIt concept]
- Hereditary optic atrophy [MedDRA Preferred Term]
- Hereditary optic atrophy [ICD-9 code]
- Hereditary optic atrophy (disorder) [SNOMED CT concept]
- hereditary optic atrophy [Disease (Nov.)]
- hereditary optic atrophy, nos [SNOMED Notion]

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