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Disease Dyschromatosis universalis hereditaria

Name Dyschromatosis universalis hereditaria
Categories Genetic disease (inborn) | Pathology (process) | Skin disease
MeSH® ID C535730
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Skin Diseases, Genetic Has associated chemicals Has associated genes Has associated exposure references Dyschromatosis universalis hereditaria
2. DiseasesSkin and Connective Tissue Diseases Has associated chemicals Has associated genes Has associated exposure references Skin Diseases Has associated chemicals Has associated genes Has associated exposure references Pigmentation Disorders Has associated chemicals Has associated genes Has associated exposure references Dyschromatosis universalis hereditaria
3. DiseasesSkin and Connective Tissue Diseases Has associated chemicals Has associated genes Has associated exposure references Skin Diseases Has associated chemicals Has associated genes Has associated exposure references Skin Diseases, Genetic Has associated chemicals Has associated genes Has associated exposure references Dyschromatosis universalis hereditaria
4. DiseasesPathological Conditions, Signs and Symptoms Has associated chemicals Has associated genes Has associated exposure references Pathologic Processes Has associated chemicals Has associated genes Has associated exposure references Pigmentation Disorders Has associated chemicals Has associated genes Has associated exposure references Dyschromatosis universalis hereditaria

Top ↑ Descendants

None.