Heterotaxy Syndrome with Polysplenia

Preferred Label : Heterotaxy Syndrome with Polysplenia;

NCIt related terms : Heterotaxy, Polysplenia;

NCIt definition : A congenital defect in which there is an abnormal spatial arrangement of the internal thoraco-abdominal organs; this manifestation of the disorder presents with many accessory spleens instead of one.;

Détails

Origin ID

C101325;

UMLS CUI

C3640087;

Automatic exact mappings (from CISMeF team)
- Polysplenia heterotaxy syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Polysplenia heterotaxy syndrome (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- Heterotaxia [ORDO Disease]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients