friedreich's ataxia

Preferred Label : friedreich's ataxia;

Détails

Origin ID

DA-22010;

UMLS CUI

C0016719;

Automatic exact mappings (from CISMeF team)
- Hereditary ataxia [MedDRA LLT]
- Hereditary ataxia [ICD-10 category]
- Hereditary ataxia [ICD-11 Subcategory]
- Hereditary ataxia [MedDRA Preferred Term]
- Hereditary ataxia [ICD-10 category (who)]
- Hereditary ataxia (disorder) [SNOMED CT concept]
- Hereditary ataxia NOS [MedDRA LLT]
- Hereditary ataxia, unspecified [ICD-10 Sub-category (who)]
- Other hereditary ataxias [ICD-10 Sub-category (who)]
- ataxias, hereditary [MeSH concept]
- friedreich's ataxia [EMDN type]
- spinocerebellar degenerations [MeSH Descriptor]
Currated CISMeF NLP mapping
- Friedreich Ataxia [NCIt concept]
- Friedreich ataxia [Radlex concept]
- Friedreich ataxia [PASCAL descriptor]
- Friedreich ataxia [DO Concept]
- Friedreich ataxia [Disease (Nov.)]
- Friedreich ataxia [ICD-11 Sub-sub category]
- Friedreich ataxia [ACR pathology]
- Friedreich ataxia [ORDO Disease]
- Friedreich ataxia [OMIM Phenotype]
- Friedreich ataxia (disorder) [SNOMED CT concept]
- Friedreich's ataxia [ICD-9 code]
- Friedreich's ataxia [MedDRA Preferred Term]
- friedreich ataxia [MeSH Descriptor]
- friedreich ataxia [MeSH concept]
- friedreich's ataxia [MedlinePlus Topic]
Décrit
- dilated cardiomyopathy secondary to friedreich's ataxia [SNOMED Notion]
- hypertrophic cardiomyopathy secondary to friedreich's ataxia [SNOMED Notion]
ICD-10 exact mapping(s)
- Early-onset cerebellar ataxia [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Autosomal recessive degenerative and progressive cerebellar ataxia [ORDO Disease]
- Cerebellar ataxia with peripheral neuropathy [ORDO Disease]
- Early-onset ataxia with dementia [ORDO Disease]
- Hereditary iron overload with neurologic manifestation [ORDO Disease]
- Neurodegenerative disease with dementia [ORDO Disease]
- Neurometabolic disease [ORDO Disease]
- Rare dementia [ORDO Disease]
- Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly [ORDO Disease]
- Syndrome associated with hypertrophic cardiomyopathy [ORDO Disease]
Metaterm(s)
- neurology [CISMeF Metaterm]
SNOMED CT concept
- Friedreich ataxia (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Friedreich Ataxia [NCIt concept]
- Friedreich ataxia [ORDO Disease]
- Friedreich ataxia [Radlex concept]
- Friedreich ataxia [Disease (Nov.)]
- Friedreich ataxia [DO Concept]
- Friedreich ataxia [OMIM Phenotype]
- Friedreich ataxia (disorder) [SNOMED CT concept]
- Friedreich's ataxia [ICD-9 code]
- Friedreich's ataxia [MedDRA Preferred Term]
- friedreich ataxia [MeSH Descriptor]
- friedreich ataxia [MeSH concept]
- friedreich's ataxia [MedlinePlus Topic]
Validated automatic mappings to BTNT
- friedreich ataxia 1 [MeSH concept]

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