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.1Y — Other specified neurofibromatoses
ICD-11 LD2D.1Y — Other specified neurofibromatoses
The diagnosis has no description.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Secondary childhood glaucoma #9882
- Neurofibromatoses #9892
- Secondary childhood glaucoma #10480
- Neurofibromatoses #10490
- Syndromic genetically-determined hypermelanosis or lentiginosis #15989
- Neurofibromatoses #15992
- 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