Disturbances of human pigmentation
ABCD syndromeAcromelanismAlbinism in humansAlbinism – black lock – cell migration disorder of the neurocytes of the gut – deafness syndromeAlbinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndromeAlbinism–deafness syndromeAlezzandrini syndromeArgyriaArsenic poisoningBismuthiaCanthaxanthinCarotenosisChloasma facieiChrysiasisChédiak–Higashi syndromeCross syndromeDark dot diseaseDermatopathia pigmentosa reticularisDermatopathia pigmentosa reticularis hyperkeratotica et mutilansDermatopathia pigmentosa reticularis hypohidotica et atrophicaDowling–Degos' diseaseDyschromatosis symmetrica hereditariaDyschromatosis universalis hereditariaDyschromiaElejalde syndromeFamilial cutaneous amyloidosisFamilial progressive hyperpigmentationFlagellate mushroom dermatitisFlagellate pigmentation from bleomycinGalli–Galli diseaseGriscelli syndromeGriscelli syndrome type 1Griscelli syndrome type 2Griscelli syndrome type 3Haber syndromeHemosiderin hyperpigmentationHereditary haemochromatosisHermansky–Pudlak syndromeHypopigmentationHypopigmentation and microphthalmia
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ABCD syndromeAcromelanismAlbinism in humansAlbinism – black lock – cell migration disorder of the neurocytes of the gut – deafness syndromeAlbinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndromeAlbinism–deafness syndromeAlezzandrini syndromeArgyriaArsenic poisoningBismuthiaCanthaxanthinCarotenosisChloasma facieiChrysiasisChédiak–Higashi syndromeCross syndromeDark dot diseaseDermatopathia pigmentosa reticularisDermatopathia pigmentosa reticularis hyperkeratotica et mutilansDermatopathia pigmentosa reticularis hypohidotica et atrophicaDowling–Degos' diseaseDyschromatosis symmetrica hereditariaDyschromatosis universalis hereditariaDyschromiaElejalde syndromeFamilial cutaneous amyloidosisFamilial progressive hyperpigmentationFlagellate mushroom dermatitisFlagellate pigmentation from bleomycinGalli–Galli diseaseGriscelli syndromeGriscelli syndrome type 1Griscelli syndrome type 2Griscelli syndrome type 3Haber syndromeHemosiderin hyperpigmentationHereditary haemochromatosisHermansky–Pudlak syndromeHypopigmentationHypopigmentation and microphthalmia
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Disturbances of human pigmentation
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Disturbances of human pigmentation
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Disturbances of human pigmentation
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