cohen syndrome

Preferred Label : cohen syndrome;

CISMeF synonym : cohen;

Details

Origin ID

D4-00616;

UMLS CUI

C0265223;

Automatic exact mappings (from CISMeF team)
- Cohen syndrome [DO Concept]
Currated CISMeF NLP mapping
- Cohen syndrome [PASCAL descriptor]
- Cohen syndrome [Disease (Nov.)]
- Cohen syndrome [ICD-11 More detail]
- Cohen syndrome [MeSH concept]
- Cohen syndrome [OMIM Phenotype]
- Cohen syndrome [MedDRA Preferred Term]
- Cohen syndrome [ORDO Disease]
- Cohen syndrome (disorder) [SNOMED CT concept]
- cohen syndrome [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Constitutional neutropenia [ORDO Disease]
- Genetic obesity [ORDO Disease]
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disability [ORDO Disease]
- Rare genetic syndromic intellectual disability [ORDO Disease]
- Rare syndromic intellectual disability [ORDO Disease]
- Syndromic myopia [ORDO Disease]
- Syndromic rod-cone dystrophy [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Cohen syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cohen syndrome [ORDO Disease]
- Cohen syndrome [MeSH concept]
- Cohen syndrome [OMIM Phenotype]
- Cohen syndrome [Disease (Nov.)]
- Cohen syndrome [PASCAL descriptor]
- Cohen syndrome [ICD-11 More detail]
- Cohen syndrome [DO Concept]
- Cohen syndrome [MedDRA Preferred Term]
- Cohen syndrome (disorder) [SNOMED CT concept]
- cohen syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

Main resources

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