ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2B — Syndromes with premature ageing appearance as a major...
ICD-11 LD2B — Syndromes with premature ageing appearance as a major feature
A heterogeneous group of hereditary syndromes in which affected individuals do or appear to age at an accelerated rate.
It includes 5 items.
- Progeroid syndromes
- Cockayne syndrome
- Rothmund-Thomson syndrome
- Progeria
- Kindler syndrome
It excludes 2 items.
- Xeroderma pigmentosum (LD27.1)
- Cutis laxa (EE41.0)
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
The diagnosis is included in 5 other classes.
- Ehlers-Danlos syndrome, progeroid type (LD28.1Y)
- Autosomal recessive cutis laxa, type 3 (LD28.2)
- Bloom syndrome (4A01.31)
- Ataxia-telangiectasia (4A01.31)
- Mandibuloacral dysplasia (LD27.6Z)