Disease_Has_Molecular_Abnormality
Disease_May_Have_Associated_Disease
Disease_Has_Associated_Disease
Disease_Mapped_To_Gene
STK11 Gene Mutation
CPTAC Terminology
CPTAC Baseline Medical Forms Terminology
GDC Terminology
CPTAC Pancreatic Baseline Form
Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia
Comorbidity
Cellosaurus Disease Terminology
Childhood Cancer Predisposition Study Terminology
CCPS Disease Terminology
GDC Value Terminology
STK11 Gene
Cellosaurus Terminology
Hereditary Neoplastic Syndrome
Peutz-Jeghers Syndrome
A genetic disorder in which polyps form in the intestine and dark spots appear on the mouth and fingers. Having Peutz-Jeghers syndrome increases the risk of developing gastrointestinal and many other types of cancer.
An inherited condition characterized by generalized hamartomatous multiple polyposis of the intestinal tract. Transmitted in an autosomal dominant fashion, Peutz-Jeghers syndrome consistently involves the jejunum and is associated with melanin spots of the lips, buccal mucosa, and fingers. This syndrome is associated with abnormalities of chromosome 19. Also known as Jeghers-Peutz syndrome and Peutz's syndrome.
C0031269
C3324
CCPS
CPTAC
Cellosaurus
Disease or Syndrome
GDC
Jeghers-Peutz Syndrome
PJS
Peutz's Syndrome
Peutz-Jeghers Disease
Peutz-Jeghers Disease
Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
Peutz-Jeghers syndrome
Peutz-Jeghers_Syndrome
Pancreatic Carcinoma
Peutz-Jeghers Polyp
Breast Carcinoma
Ovarian Carcinoma
Small Intestinal Carcinoma
Cervical Carcinoma
Malignant Testicular Germ Cell Tumor