Search Ontology:
Human Disease
Peutz-Jeghers syndrome
- Term ID
- DOID:3852
- Synonyms
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- 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
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models