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)

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