Obesity due to congenital leptin deficiency

Preferred Label : Obesity due to congenital leptin deficiency;

ICD-11 definition : Congenital leptin deficiency is a form of monogenic obesity characterised by severe early-onset obesity and marked hyperphagia.;

Details

Origin ID

591009309;

UMLS CUI

C3554224;

Currated CISMeF NLP mapping
- Leptin deficiency or dysfunction [OMIM Phenotype]
- Obesity due to congenital leptin deficiency [ORDO Disease]
- congenital leptin deficiency [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital leptin deficiency [MedDRA Preferred Term]
- Congenital leptin deficiency (disorder) [SNOMED CT concept]
- Leptin Deficiency [NCIt concept]
- Leptin deficiency or dysfunction [OMIM Phenotype]
- Obesity due to congenital leptin deficiency [ORDO Disease]
- congenital leptin deficiency [DO Concept]
- leptin deficiency [Disease (Nov.)]
Validated automatic mappings to NTBT
- Leptin Deficiency [NCIt concept]
- leptin deficiency [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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