EC23.0
category
Non-syndromic genetically-determined hypermelanosis or lentiginosis
Also indexed as
Café-au-lait spots syndromeCentrofacial lentiginosisDowling-Degos diseaseFamilial generalised lentiginosisFamilial multiple café-au-lait maculesFamilial progressive hyperpigmentationGalli-Galli diseaseHypermelanotic pigmentary mosaicismInherited patterned lentiginosisLinear or whorled naevoid hypermelanosisNF6 - [Neurofibromatosis type 6]Neurofibromatosis type 6Non-syndromic genetically-determined hypermelanosis or lentiginosisPartial unilateral lentiginosisReticulate pigmented anomaly of the flexuresSegmental lentiginosis
Nearby in Genetic disorders of skin pigmentation