EH40.2 Erythrodermas of infancy

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

code elsewhere

• Severe combined immunodeficiency with hypereosinophilia  (4A01.10)
• Wiskott-Aldrich syndrome  (3B62.0Y)
• Congenital non-bullous ichthyosiform erythroderma  (EC20.02)
• Netherton syndrome  (LD27.2)
• Multiple carboxylase deficiency due to holocarboxylase synthetase deficiency  (5C50.E0)

synonyms

• Erythrodermas of infancy
• Congenital erythroderma of uncertain nature
• Leiner disease

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