congenital disease, nos

Preferred Label : congenital disease, nos;

Details

Origin ID

D4-00000;

UMLS CUI

C0242354;

Automatic exact mappings (from CISMeF team)
- Congenital clinodactyly (disorder) [SNOMED CT concept]
- Congenital disease [PASCAL descriptor]
- Congenital disorder due to abnormality of chromosome number OR structure (disorder) [SNOMED CT concept]
- Congenital disorders [HPMULTI term]
- Congenital hamartoma (disorder) [SNOMED CT concept]
- Congenital malposition of eye (disorder) [SNOMED CT concept]
- Congenital malposition of pubis (disorder) [SNOMED CT concept]
- Congenital malrotation (morphologic abnormality) [SNOMED CT concept]
- Congenital miosis (disorder) [SNOMED CT concept]
- Congenital short trunk (disorder) [SNOMED CT concept]
- congenital disease [COVID-19 Thesaurus concept]
- developmental anomaly [Artificial nutrition thesaurus concept]
- for congenital disease [LOINC component]
Currated CISMeF NLP mapping
- Congenital [NCIt concept]
- Congenital disease [LOINC part]
- Congenital disease (disorder) [SNOMED CT concept]
- congenital disorder [Radlex concept]
- congenital disorders [MeSH concept]
Décrit
- congenital human immunodeficiency virus infection [SNOMED Notion]
- congenital infectious disease, nos [SNOMED Notion]
- congenital viral hepatitis b infection [SNOMED Notion]
ICD-10 exact mapping(s)
- Congenital malformation, unspecified [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Congenital disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital disease [LOINC part]
- Congenital disease (disorder) [SNOMED CT concept]
- congenital disorders [MeSH concept]

Keyword's position in hierarchy(ies) :

Main resources

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