N syndrome - CISMeF

CISMeF

chu

N syndromeMeSH Supplementary Concept

Preferred Label : N syndrome;

MeSH note : Mental retardation, malformations, chromosome breakage, and development of T-cell leukemia;

Details

Origin ID

C536108;

UMLS CUI

C2936859;

Currated CISMeF NLP mapping
- N syndrome [DO Concept]
- N syndrome [ICD-11 More detail]
- N syndrome [OMIM Phenotype]
- N syndrome [ORDO Disease]
- N syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- DNA Repair-Deficiency disorders [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- leukemia, t-cell [MeSH Descriptor]
ORDO relation(s)
- N syndrome [ORDO Disease]
Record concept(s)
- N syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- N syndrome [ORDO Disease]
- N syndrome [OMIM Phenotype]
- N syndrome [DO Concept]
- N syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
02/05/2025

© Rouen University Hospital. Any partial or total use of this material must mention the source.