Hydranencephaly

Preferred Label : Hydranencephaly;

NCIt definition : A rare congenital brain disorder in which the cerebral hemispheres are absent and replaced by sacs that contain cerebrospinal fluid. Signs and symptoms include irritability, increased muscle tone, seizures, and hydrocephalus. The prognosis is poor.;

Détails

Origin ID

C98949;

UMLS CUI

C0020225;

Automatic exact mappings (from CISMeF team)
- Hydranencephaly [ICD-11 Sub-sub category]
Currated CISMeF NLP mapping
- Hydranencephaly [ORDO Disease]
- Hydranencephaly [ACR pathology]
- Hydranencephaly [HRDO Sign]
- Hydranencephaly [MedDRA Preferred Term]
- Hydranencephaly [HPO term]
- Hydranencephaly [PASCAL descriptor]
- Hydranencephaly (disorder) [SNOMED CT concept]
- Other reduction deformities of brain [ICD-10 Sub-category (who)]
- Other reduction deformities of brain [ICD-10 Sub-category]
- hydranencephaly [SNOMED Notion]
- hydranencephaly [Disease (Nov.)]
- hydranencephaly [MeSH Descriptor]
- hydranencephaly [DO Concept]
- hydranencephaly [MeSH concept]
DO Cross reference
- hydranencephaly [DO Concept]
Has associated anatomic sites
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Hydranencephaly [MedDRA Preferred Term]
- Hydranencephaly [ORDO Disease]
- Hydranencephaly [HPO term]
- Hydranencephaly (disorder) [SNOMED CT concept]
- Other reduction deformities of brain [ICD-10 Sub-category (who)]
- hydranencephaly [SNOMED Notion]
- hydranencephaly [MeSH concept]
- hydranencephaly [MeSH Descriptor]
- hydranencephaly [DO Concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Congenital Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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