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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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