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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