Gardner syndrome

ICD-11 code : LD2D.3;

Preferred Label : Gardner syndrome;

ICD-11 definition : 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 tumors. Gardner syndrome is a term used to refer to patients in whom these extraintestinal features are unusually prominent.;

Details

Origin ID

1428130769;

Currated CISMeF NLP mapping
- Familial adenomatous polyposis 1 [OMIM Phenotype]
- Gardner Syndrome [NCIt concept]
- Gardner syndrome [PASCAL descriptor]
- Gardner syndrome [ORDO Disease]
- Gardner syndrome (disorder) [SNOMED CT concept]
- Gardner's syndrome [MedDRA LLT]
- gardner syndrome [SNOMED Notion]
- gardner syndrome [MeSH concept]
- gardner syndrome [MeSH Descriptor]
ICD-10 Mapping
- Phakomatoses, not elsewhere classified [ICD-10 category]
Validated automatic mappings to NTBT
- Phakomatoses, not elsewhere classified [ICD-10 category]

Keyword's position in hierarchy(ies) :

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