ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2D — Phakomatoses or hamartoneoplastic syndromes
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
- Polyposis syndrome #2669
- 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