ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD27 — Syndromes with skin or mucosal anomalies as a major feature
LD27.5 — Genetic hamartoneoplastic syndromes affecting the skin
LD2D.1 — Neurofibromatoses
LD2D.11 — Neurofibromatosis type 2
ICD-11 LD2D.11 — Neurofibromatosis type 2
Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development of multiple schwannomas and meningiomas.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Inherited cancer-predisposing syndromes #2829
- Neurofibromatoses #9892
- Neurofibromatoses #10490
- Neurofibromatoses #15992
- Neurofibromatoses #16082
- Neurofibromatoses #16280
- Neurofibromatoses #22318
- Neurofibromatoses #23397