Familial dysautonomia [Riley-Day]

Preferred Label : Familial dysautonomia [Riley-Day];

Diag associé à un acte (%) : 74.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

G901;

UMLS CUI

C0013364;

Currated CISMeF NLP mapping
- Familial Dysautonomia [NCIt concept]
- Familial dysautonomia [MedDRA LLT]
- Familial dysautonomia [PASCAL descriptor]
- Familial dysautonomia [ORDO Disease]
- Familial dysautonomia (disorder) [SNOMED CT concept]
- Familial dysautonomia [Riley-Day] [ICD-10 Sub-category (who)]
- Hereditary sensory and autonomic neuropathy type III [ICD-11 Subcategory]
- Neuropathy, hereditary sensory and autonomic, type III [OMIM Phenotype]
- Riley-Day syndrome [DO Concept]
- Riley-Day syndrome [MedDRA Preferred Term]
- dysautonomia, familial [MeSH Descriptor]
- dysautonomia, familial [MeSH concept]
- familial dysautonomia [SNOMED Notion]
- familial dysautonomia [Radlex concept]
- familial dysautonomia [Disease (Nov.)]
DO Cross reference
- Riley-Day syndrome [DO Concept]
Excluded by
- Other congenital malformations of nervous system [ICD-10 category]
- Phakomatoses, not elsewhere classified [ICD-10 category]
Orphanet concepts
- Familial dysautonomia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial Dysautonomia [NCIt concept]
- Familial dysautonomia [MedDRA LLT]
- Familial dysautonomia [ORDO Disease]
- Familial dysautonomia [PASCAL descriptor]
- Familial dysautonomia (disorder) [SNOMED CT concept]
- Hereditary sensory and autonomic neuropathy type III [ICD-11 Subcategory]
- Neuropathy, hereditary sensory and autonomic, type III [OMIM Phenotype]
- Riley-Day syndrome [MedDRA Preferred Term]
- Riley-Day syndrome [DO Concept]
- dysautonomia, familial [MeSH Descriptor]
- dysautonomia, familial [MeSH concept]
- familial dysautonomia [Radlex concept]
- familial dysautonomia [SNOMED Notion]
- familial dysautonomia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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