Neuronal intranuclear inclusion disease

Preferred Label : Neuronal intranuclear inclusion disease;

ICD-11 definition : Neuronal intranuclear inclusion disease is a very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic intranuclear inclusions in neuronal and glial cells, and neuronal loss. Infantile, juvenile, and adult-onset cases have been described.;

Details

Origin ID

693937860;

UMLS CUI

C1863843;

Automatic exact mappings (from CISMeF team)
- Neuronal intranuclear inclusion disease [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Neuronal Intranuclear Inclusion Disease [NCIt concept]
- Neuronal intranuclear inclusion disease [OMIM Phenotype]
- Neuronal intranuclear inclusion disease [MeSH concept]
- Neuronal intranuclear inclusion disease [ORDO Disease]
- Neuronal intranuclear inclusion disease (disorder) [SNOMED CT concept]
- neuronal intranuclear inclusion disease [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuronal Intranuclear Inclusion Disease [NCIt concept]
- Neuronal intranuclear inclusion disease [OMIM Phenotype]
- Neuronal intranuclear inclusion disease [MeSH concept]
- Neuronal intranuclear inclusion disease [ORDO Disease]
- Neuronal intranuclear inclusion disease [MedDRA Preferred Term]
- Neuronal intranuclear inclusion disease (disorder) [SNOMED CT concept]
- neuronal intranuclear inclusion disease [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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