LD27.5 Genetic hamartoneoplastic syndromes affecting the skin
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A heterogeneous group of inherited diseases characterised by the presence of multiple hamartomata and associated with an increased risk of malignancy.
code elsewhere
- Neurofibromatoses (LD2D.1)
- Tuberous sclerosis (LD2D.2)
- Gardner syndrome (LD2D.3)
- Gorlin syndrome (LD2D.4)
- Bannayan-Riley-Ruvalcaba syndrome (LD2D.Y)
- Cowden syndrome (LD2D.Y)
- Multiple familial trichoepithelioma (2F22)
synonyms
- Genetic hamartoneoplastic syndromes affecting the skin
- Legius syndrome
- NF1-like syndrome
- Neurofibromatosis 1-like syndrome
- NFLS - [Neurofibromatosis 1-like syndrome] (MIM 611431)
- Bazex-Dupré-Christol syndrome
- Follicular atrophoderma and basal cell carcinoma syndrome [Bazex]
- Birt-Hogg-Dubé syndrome
- Fibrofolliculomas with trichodiscomas and acrochordons
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