Cohen syndrome

Preferred Label : Cohen syndrome;

ICD-11 definition : Cohen syndrome is a genetic syndrome characterized by obesity, hypotonia, intellectual deficit, characteristic craniofacial dysmorphism and abnormalities of the hands and feet.;

Détails

Origin ID

1188737383;

UMLS CUI

C0265223;

Automatic exact mappings (from CISMeF team)
- Cohen syndrome [DO Concept]
Currated CISMeF NLP mapping
- Cohen syndrome [OMIM Phenotype]
- Cohen syndrome [MedDRA Preferred Term]
- Cohen syndrome [PASCAL descriptor]
- Cohen syndrome [MeSH concept]
- Cohen syndrome [ORDO Disease]
- Cohen syndrome [Disease (Nov.)]
- Cohen syndrome (disorder) [SNOMED CT concept]
- cohen syndrome [SNOMED Notion]
- cohen syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cohen syndrome [MedDRA Preferred Term]
- Cohen syndrome [OMIM Phenotype]
- Cohen syndrome [MeSH concept]
- Cohen syndrome [Disease (Nov.)]
- Cohen syndrome [ORDO Disease]
- Cohen syndrome [PASCAL descriptor]
- Cohen syndrome [DO Concept]
- Cohen syndrome (disorder) [SNOMED CT concept]
- cohen syndrome [MeSH Supplementary Concept]
- cohen syndrome [SNOMED Notion]

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

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