optic atrophy - CISMeF

Preferred Label : optic atrophy;

MeSH definition : Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.;

MeSH synonym : atrophy, optic;

Wikipedia automatic translation : Optic neuropathy;

MeSH annotation : /genet permitted but do not confuse with OPTIC ATROPHIES, HEREDITARY;

Wikipedia link : https://en.wikipedia.org/wiki/Optic neuropathy;

Details

Origin ID

D009896;

UMLS CUI

C0029124;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [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]
Automatic exact mappings (from CISMeF team)
- Atrophy optic nerve [MedDRA LLT]
- Optic nerve atrophy [PASCAL descriptor]
Currated CISMeF NLP mapping
- Atrophy optic [MedDRA LLT]
- Genetic optic atrophy [ORDO Disease]
- OPTIC ATROPHY [WHO-ART Preferred Term]
- Optic Atrophy [NCIt concept]
- Optic atrophy [ICD-10 Sub-category]
- Optic atrophy [ICD-11 Subcategory]
- Optic atrophy [HPO term]
- Optic atrophy [ICD-9 code]
- Optic atrophy [ICD-10 Sub-category (who)]
- Optic atrophy [MedDRA Preferred Term]
- Optic atrophy [OMIM phenotypic series]
- Optic atrophy (disorder) [SNOMED CT concept]
- optic atrophy [DO Concept]
- optic atrophy [Disease (Nov.)]
- optic atrophy, nos [SNOMED Notion]
DO Cross reference
- optic atrophy [DO Concept]
HPO term
- Optic atrophy [HPO term]
Manual BTNT mappings - CISMeF
- Autosomal dominant optic atrophy [ORDO Disease]
- Autosomal recessive optic atrophy [ORDO Disease]
- X-linked recessive optic atrophy [ORDO Disease]
Record concept(s)
- optic atrophy [MeSH concept]
Related MeSH Supplementary Concept(s)
- Al Gazali Sabrinathan Nair syndrome [MeSH Supplementary Concept]
- CAPOS syndrome [MeSH Supplementary Concept]
- Mohr-Tranebjaerg syndrome [MeSH Supplementary Concept]
- PEHO syndrome [MeSH Supplementary Concept]
- X-linked mental retardation gustavson type [MeSH Supplementary Concept]
- al gazali khidr prem chandran syndrome [MeSH Supplementary Concept]
- behr syndrome [MeSH Supplementary Concept]
- costeff optic atrophy syndrome [MeSH Supplementary Concept]
- jensen syndrome [MeSH Supplementary Concept]
- mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature [MeSH Supplementary Concept]
- optic atrophy, X-linked [MeSH Supplementary Concept]
- optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant [MeSH Supplementary Concept]
- silengo lerone pelizza syndrome [MeSH Supplementary Concept]
- spastic ataxia [MeSH Supplementary Concept]
- spastic paraplegia, optic atrophy, and neuropathy [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- warburg sjo fledelius syndrome [MeSH Supplementary Concept]
- wolfram syndrome 2 [MeSH Supplementary Concept]
SNOMED CT : Morphologiquement associé
- atrophy [MeSH Descriptor]
See also (suggested by CISMeF)
- optic atrophies, hereditary [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrophy optic [MedDRA LLT]
- Atrophy optic nerve [MedDRA LLT]
- Genetic optic atrophy [ORDO Disease]
- OPTIC ATROPHY [WHO-ART Preferred Term]
- Optic Atrophy [NCIt concept]
- Optic atrophy [ICD-9 code]
- Optic atrophy [ICD-10 Sub-category]
- Optic atrophy [HPO term]
- Optic atrophy [ICD-10 Sub-category (who)]
- Optic atrophy [MedDRA Preferred Term]
- Optic atrophy (disorder) [SNOMED CT concept]
- Optic atrophy, unspecified [MedDRA LLT]
- Optic atrophy, unspecified [ICD-9 code]
- optic atrophy [DO Concept]
- optic atrophy [Disease (Nov.)]
- optic atrophy, nos [SNOMED Notion]

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