ICD-11 classes
14 Diseases of the skin
Genetic and developmental disorders affecting the skin
EC23 — Genetic disorders of skin pigmentation
EC23.1 — Syndromic genetically-determined hypermelanosis or...
LD2D.1 — Neurofibromatoses
ICD-11 LD2D.1 — Neurofibromatoses
The neurofibromatoses (NF) are related genetic disorders which affect bone, soft tissue, skin and nervous system. In NF type 1 neurofibromas develop in the skin and elsewhere: these can cause problems as a result of their visibility in the skin, compression of vital internal structures or from malignant degeneration. Neuromas of the acoustic nerve are the predominant problem in NF type 2.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code LD2D.1 contains 5 clarifying diagnoses:
- LD2D.10 — Neurofibromatosis type 1
- LD2D.11 — Neurofibromatosis type 2
- LD2D.12 — Neurofibromatosis type 3
- LD2D.1Y — Other specified neurofibromatoses
- LD2D.1Z — Neurofibromatosis, unspecified
The diagnosis is coded elsewhere:
- Secondary childhood glaucoma #9882
- Neurofibromatoses #9892
- Secondary childhood glaucoma #10480
- Neurofibromatoses #10490
- Genetic hamartoneoplastic syndromes affecting the skin #16081
- Neurofibromatoses #16082
- Syndromic genetically-determined hypermelanosis or lentiginosis #16277
- Neurofibromatoses #16280
- Secondary childhood glaucoma #22308
- Neurofibromatoses #22318
- Genetic hamartoneoplastic syndromes affecting the skin #23341
- Neurofibromatoses #23342
- Phakomatoses or hamartoneoplastic syndromes #23395
- Neurofibromatoses #23397