Hereditary ataxia, unspecified

Preferred Label : Hereditary ataxia, unspecified;

Inclusion CIM-10 : Hereditary cerebellar ataxia NOS; Hereditary cerebellar degeneration; Hereditary cerebellar disease; Hereditary cerebellar syndrome;

Diag associé à un acte (%) : 72.0;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G119;

UMLS CUI

C5779602;

Automatic exact mappings (from CISMeF team)
- Hereditary cerebellar degeneration (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary ataxia [MedDRA LLT]
- Hereditary ataxia [PASCAL descriptor]
- Hereditary ataxia [ICD-11 Subcategory]
- Hereditary ataxia [MedDRA Preferred Term]
- Hereditary ataxia (disorder) [SNOMED CT concept]
- Hereditary ataxia NOS [MedDRA LLT]
- Rare hereditary ataxia [ORDO Disease]
- ataxias, hereditary [MeSH concept]
- hereditary ataxia [DO Concept]
Validated automatic mappings to NTBT
- Hereditary ataxia (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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