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Disease Ontology Browser
Peutz-Jeghers syndrome (DOID:3852)
Alliance: disease page
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
Alt IDs: OMIM:175200, DOID:4133, DOID:4134, DOID:6252, DOID:6253, ICD10CM:Q85.89, MESH:D010580, NCI:C3324, NCI:C4733, NCI:C7755, ORDO:2869, UMLS_CUI:C0031269, UMLS_CUI:C0265323, UMLS_CUI:C0456487
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.

Disease References using Mouse Models (9)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory