ICD-11 classes
14 Diseases of the skin
Skin disorders involving specific cutaneous structures
Disorders of the dermis and subcutis
Disorders of cutaneous connective tissue
Poikiloderma
EC10 — Genetic syndromes with poikiloderma
ICD-11 EC10 — Genetic syndromes with poikiloderma
Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
The diagnosis is included in 6 other classes.
- Cockayne syndrome (LD2B)
- Rothmund-Thomson syndrome (LD2B)
- Hereditary acrokeratotic poikiloderma, Weary type (LD27.Y)
- Kindler syndrome (LD2B)
- Bloom syndrome (4A01.31)
- Dyskeratosis congenita (3A70.0)