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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