Obesity due to leptin receptor gene deficiency

Preferred Label : Obesity due to leptin receptor gene deficiency;

Origin ID

997823205;

UMLS CUI

C3554225;

Currated CISMeF NLP mapping
- Leptin receptor deficiency [OMIM Phenotype]
- Obesity due to leptin receptor gene deficiency [ORDO Disease]
- Obesity due to leptin receptor gene deficiency (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- Leptin Receptor Deficiency [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Leptin Receptor Deficiency [NCIt concept]
- Leptin receptor deficiency [OMIM Phenotype]
- Leptin receptor deficiency [MedDRA Preferred Term]
- Obesity due to leptin receptor gene deficiency [ORDO Disease]