Search Ontology:
Human Disease

Peutz-Jeghers syndrome

Term ID
DOID:3852
Synonyms
  • Colonic hamartomatous polyp
  • gastric Peutz-Jeghers polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • 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. (2)
References
  • GARD:7378
  • ICD10CM:Q85.89
  • MESH:D010580
  • MIM:175200
  • NCI:C3324
  • NCI:C4733
  • NCI:C7755
  • ORDO:2869
  • SNOMEDCT_US_2023_03_01:157029009
  • SNOMEDCT_US_2023_03_01:277161008
  • SNOMEDCT_US_2023_03_01:53633000
  • UMLS_CUI:C0031269
  • UMLS_CUI:C0265323
  • UMLS_CUI:C0456487
Ontology
Human Disease   ( DOID:3852 )
Relationships
is a type of
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Genes Involved
Zebrafish Models