obesity, hyperphagia, and developmental delay

Preferred Label : obesity, hyperphagia, and developmental delay;

MeSH note : mutation in NTRK2;

Origin ID

C563938;

UMLS CUI

C3151303;

Currated CISMeF NLP mapping
- Obesity, hyperphagia, and developmental delay [OMIM Phenotype]
MeSH term(s) associated for indexing
- developmental disabilities [MeSH Descriptor]
- hyperphagia [MeSH Descriptor]
- obesity [MeSH Descriptor]
Record concept(s)
- obesity, hyperphagia, and developmental delay [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Obesity, hyperphagia, and developmental delay [OMIM Phenotype]