Peutz-Jeghers syndrome

Summary
Synonym
  • Colonic hamartomatous polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • gastric Peutz-Jeghers polyp
  • peutz-jeghers small bowel hamartoma
Definition
An intestinal disease characterized by melanocytic macules of the lips, buccal mucosa, and digits; multiple gastrointestinal hamartomatous polyps; and an increased risk of various neoplasms that has_material_basis_in heterozygous mutation in the serine/threonine kinase STK11 gene on chromosome 19p13.
Super Class
intestinal disease
External Links
Disease Ontology
DOID:3852
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 25 in total
Gene ID Gene Symbol Description Source
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5563 PRKAA2 protein kinase AMP-activated catalytic subunit alpha 2
5728 PTEN phosphatase and tensin homolog
5743 PTGS2 prostaglandin-endoperoxide synthase 2
5837 PYGM glycogen phosphorylase, muscle associated
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6391 SDHC succinate dehydrogenase complex subunit C
6392 SDHD succinate dehydrogenase complex subunit D

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024