ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD27 — Syndromes with skin or mucosal anomalies as a major feature
LD27.6 — Genetic lipodystrophy
ICD-11 LD27.6 — Genetic lipodystrophy
Genetic lipodystrophies represent a heterogeneous group of rare diseases characterised by a generalised or localised loss of body fat (lipoatrophy).
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code LD27.6 contains 2 clarifying diagnoses:
- LD27.60 — Congenital generalised lipodystrophy
- LD27.6Z — Genetic lipodystrophy, unspecified
The diagnosis is coded elsewhere:
- Genetic disorders of adipose tissue or lipid metabolism affecting the skin #16063
- Genetic lipodystrophy #16067
- Lipoatrophy or lipodystrophy #16546
- Genetic lipodystrophy #16549
The diagnosis is included in 2 other classes.
- Familial partial lipodystrophy (5A44)
- Wiedemann-Rautenstrauch progeroid syndrome (LD2B)