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EC10 Genetic syndromes with poikiloderma

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.

code elsewhere

• 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)

synonyms

• Genetic syndromes with poikiloderma
• Poikiloderma with neutropaenia
• Poikiloderma with neutropaenia, Clericuzio type
• Hereditary sclerosing poikiloderma
• Hereditary sclerosing poikiloderma (MIM 173700)
• Hereditary sclerosing poikiloderma, Weary type
• Hereditary sclerosing poikiloderma with cardiac anomalies
• Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
• Congenital or hereditary poikiloderma of uncertain or unspecified type

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