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
ICD-11 LD27.5 — Genetic hamartoneoplastic syndromes affecting the skin
A heterogeneous group of inherited diseases characterised by the presence of multiple hamartomata and associated with an increased risk of malignancy.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code LD27.5 contains 4 clarifying diagnoses:
- LD2D.1 — Neurofibromatoses
It contains 5 clarifying diagnoses. - LD2D.2 — Tuberous sclerosis
- LD2D.3 — Gardner syndrome
- LD2D.4 — Gorlin syndrome
The diagnosis is coded elsewhere:
The diagnosis is included in 7 other classes.
- Neurofibromatoses (LD2D.1)
- Tuberous sclerosis (LD2D.2)
- Gardner syndrome (LD2D.3)
- Gorlin syndrome (LD2D.4)
- Bannayan-Riley-Ruvalcaba syndrome (LD2D.Y)
- Cowden syndrome (LD2D.Y)
- Multiple familial trichoepithelioma (2F22)