Peutz-Jeghers Syndrome (PJS)

Alias:
Pjs
Polyposis, Hamartomatous Intestinal
Polyps-and-Spots Syndrome
Hamartomatous Intestinal Polyposis
Hamartomatous Polyp
Intestinal Polyposis-Cutaneous Pigmentation Syndrome
Peutz-Jeghers Polyp of Small Intestine
Peutz-Jeghers Small Bowel Hamartoma
Periorificial Lentiginosis Syndrome
Peutz-Jeghers Polyps of Small Bowel
Intestinal Hamartomatous Polyposis
Peutz-Jeghers Polyp of the Stomach
Colonic Hamartomatous Polyp
Gastric Peutz-Jeghers Polyp
Peutz Jeghers Colon Polyp
Polyposis, Intestinal, Ii
Peutz-Jeghers Polyposis
Lentiginosis, Perioral
Peutz Jeghers Polyp
Peutz-Jeghers Polyp
Peutz Jehgers Polyp
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Peutz-Jeghers Syndrome, also known as pjs, is related to gastric cancer and cowden syndrome 1. An important gene associated with Peutz-Jeghers Syndrome is STK11 (Serine/Threonine Kinase 11), and among its related pathways/superpathways are Infectious disease and ERK Signaling. The drugs Anti-Bacterial Agents and Antifungal Agents have been mentioned in the context of this disorder. Affiliated tissues include small intestine and skin, and related phenotypes are macule and multiple lentigines
Related ID:
MESH:D010580
ICD11:1331537078

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
1-9/1000000
31
507
226

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
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