ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2D — Phakomatoses or hamartoneoplastic syndromes
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:

  1. LD2D.10 — Neurofibromatosis type 1
  2. LD2D.11 — Neurofibromatosis type 2
  3. LD2D.12 — Neurofibromatosis type 3
  4. LD2D.1Y — Other specified neurofibromatoses
  5. LD2D.1Z — Neurofibromatosis, unspecified

The diagnosis is coded elsewhere:

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