EC23.0 Non-syndromic genetically-determined hypermelanosis or lentiginosis

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

synonyms

• Non-syndromic genetically-determined hypermelanosis or lentiginosis
• Familial progressive hyperpigmentation
• Familial generalised lentiginosis
• Inherited patterned lentiginosis
• Centrofacial lentiginosis
• Familial multiple café-au-lait macules
• Café-au-lait spots syndrome
• Neurofibromatosis type 6
• NF6 - [Neurofibromatosis type 6]
• Dowling-Degos disease
• Reticulate pigmented anomaly of the flexures
• Galli-Galli disease
• Hypermelanotic pigmentary mosaicism
• Linear or whorled naevoid hypermelanosis
• Segmental lentiginosis
• Partial unilateral lentiginosis

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