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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