Prader-Willi syndrome

Summary
Synonym
  • Prader Willi syndrome
Definition
A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity.
Super Class
chromosomal disease syndrome
Disease Ontology
DOID:11983
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
3358 HTR2C 5-hydroxytryptamine receptor 2C
51738 GHRL ghrelin and obestatin prepropeptide
54551 MAGEL2 MAGE family member L2
Displaying 1 entry
Gene ID Gene Symbol Description Source
15560 Htr2c 5-hydroxytryptamine (serotonin) receptor 2C
Displaying 1 entry
Gene ID Gene Symbol Description Source
25187 Htr2c 5-hydroxytryptamine receptor 2C

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Acknowledgements

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Last updated: December 9, 2024