ICD-11 classes
02 Neoplasms
Benign neoplasms, except of lymphoid, haematopoietic,...
Benign non-mesenchymal neoplasms
2E92 — Benign neoplasm of digestive organs
2E92.4 — Benign neoplasm of the large intestine
2E92.40 — Polyposis syndrome
LD2D.3 — Gardner syndrome
ICD-11 LD2D.3 — Gardner syndrome
Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, hepatoblastoma, osteomas of the mandible and skull, epidermal cysts, and desmoid tumours. Gardner syndrome is a term used to refer to patients in whom these extraintestinal features are unusually prominent.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Malignant neoplasms of colon #2006
- Inherited cancer-predisposing syndromes #2829
- Malignant neoplasms of colon #14108
- Polyposis syndrome #14141
- Polyposis syndrome #14174
- Genetic hamartoneoplastic syndromes affecting the skin #16081
- Genetic hamartoneoplastic syndromes affecting the skin #23341
- Phakomatoses or hamartoneoplastic syndromes #23395