Aicardi Syndrome

Preferred Label : Aicardi Syndrome;

NCIt definition : A sporadic genetic syndrome characterized by agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae. It is associated with the presence of choroid plexus neoplasms in the brain.;

Details

Origin ID

C35256;

UMLS CUI

C0175713;

Currated CISMeF NLP mapping
- Aicardi syndrome [PASCAL descriptor]
- Aicardi syndrome [DO Concept]
- Aicardi syndrome [Disease (Nov.)]
- Aicardi syndrome [ICD-11 More detail]
- Aicardi syndrome [OMIM Phenotype]
- Aicardi syndrome [ORDO Disease]
- Aicardi's syndrome [MedDRA Preferred Term]
- Aicardi's syndrome (disorder) [SNOMED CT concept]
- aicardi syndrome [MeSH Descriptor]
- aicardi syndrome [MeSH concept]
- aicardi's syndrome [SNOMED Notion]
DO Cross reference
- Aicardi syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aicardi syndrome [ORDO Disease]
- Aicardi syndrome [OMIM Phenotype]
- Aicardi syndrome [PASCAL descriptor]
- Aicardi syndrome [DO Concept]
- Aicardi syndrome [Disease (Nov.)]
- Aicardi's syndrome [MedDRA Preferred Term]
- Aicardi's syndrome (disorder) [SNOMED CT concept]
- aicardi syndrome [MeSH concept]
- aicardi syndrome [MeSH Descriptor]
- aicardi's syndrome [SNOMED Notion]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_may_have_associated_disease
- Choroid Plexus Papilloma [NCIt concept]

Keyword's position in hierarchy(ies) :

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