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LD2D Phakomatoses or hamartoneoplastic syndromes

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

exclusions

• Ataxia-telangiectasia  (4A01.31)
• familial dysautonomia [Riley-Day]  (8C21.1)
• Rendu-Osler-Weber disease  (LA90.00)
• Proteus syndrome  (LD2C)
• Sturge-Weber syndrome  (LD23)
• Enchondromatosis  (2E83)
• Maffucci syndrome  (LD2F.1)
• Angio-osteohypertrophic syndrome  (LD26.60)

code elsewhere

• NAME syndrome  (2F01)
• Von Hippel-Lindau disease  (5A75)
• Focal dermal hypoplasia  (LD27.0Y)
• Epidermal naevus syndrome  (LC02)
• Lumbosacral dermal melanocytosis  (LC10)
• Naevus of Ota  (LC10)
• Naevus of Ito  (LC10)
• Dermal melanocyte hamartoma  (LC10)
• Hereditary leiomyomatosis and renal cell cancer  (2C90.Y)

sections/codes in this section (LD2D-LD2D)

• Peutz-Jeghers syndrome  (LD2D.0)
• Neurofibromatoses  (LD2D.1)
• Tuberous sclerosis  (LD2D.2)
• Gardner syndrome  (LD2D.3)
• Gorlin syndrome  (LD2D.4)
• Other specified phakomatoses or hamartoneoplastic syndromes  (LD2D.Y)
• Phakomatoses or hamartoneoplastic syndromes, unspecified  (LD2D.Z)

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