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About: Dyschromatosis universalis hereditaria     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : umbel-rc:AilmentCondition, within Data Space : dbpedia.org associated with source document(s)

Type: ThingDiseaseyago:Abstraction100002137yago:Act100030358yago:Activity100407535yago:Attribute100024264yago:Condition113920835yago:Disease114070360yago:Event100029378yago:IllHealth114052046yago:Illness114061805yago:PathologicalState114051917yago:Perturbation107428450yago:PhysicalCondition114034177yago:PsychologicalFeature100023100yago:YagoPermanentlyLocatedEntitydiseaseyago:State100024720yago:WikicatDisturbancesOfHumanPigmentationumbel-rc:AilmentCondition New Facet based on Instances of this Class

Dyschromatosis universalis hereditaria is a rare genodermatosis characterized by reticulate hyper- and hypo- pigmentated macules in a generalized distribution. Both autosomal dominant and recessive inheritance have been reported with the disorder. It has been associated with mutations in genes SASH1 and ABCB6.