congenital leptin deficiency

Summary
Synonym
  • LEPD
  • leptin deficiency or dysfunction
  • obesity due to congenital leptin deficiency
Definition
A syndrome characterized by severe early-onset obesity, hyperphagia, hypogonadotropic hypogonadism, and neuroendocrine and metabolic dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in LEP on chromosome 7q32.1.
Super Class
autosomal recessive disease physical disorder syndrome
External Links
Disease Ontology
DOID:0111334
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3952 LEP leptin
Displaying 1 entry
Gene ID Gene Symbol Description Source
16846 Lep leptin
Displaying 1 entry
Gene ID Gene Symbol Description Source
25608 Lep leptin

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024