ICD-11 classes
02 Neoplasms
Inherited cancer-predisposing syndromes
LD2D.0 — Peutz-Jeghers syndrome
ICD-11 LD2D.0 — Peutz-Jeghers syndrome
Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterised by intestinal hamartomatous polyps in association with a distinct pattern of skin and mucosal macular melanin deposition. Patients have an increased risk of developing intestinal cancer.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Polyposis syndrome #2669
- Genetic or developmental disorders involving lips or oral mucosa #13302
- Polyposis syndrome #14141
- Polyposis syndrome #14174
- Genetic or developmental disorders involving lips or oral mucosa #15229
- Syndromic genetically-determined hypermelanosis or lentiginosis #15989
- Syndromic genetically-determined hypermelanosis or lentiginosis #16277
- Genetic or developmental disorders involving lips or oral mucosa #16873
- Genetic or developmental disorders involving lips or oral mucosa #22812
- Phakomatoses or hamartoneoplastic syndromes #23395