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Disease Vohwinkel Syndrome, Variant Form

Name Vohwinkel Syndrome, Variant Form
Synonyms LORICRIN KERATODERMA | Mutilating Keratoderma with Ichthyosis | Vohwinkel Syndrome with Ichthyosis
Categories Genetic disease (inborn) | Skin disease
MeSH® ID C565826
OMIM® ID 604117

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 Vohwinkel Syndrome, Variant Form Has associated chemicals Has associated genes
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 Skin Diseases, Genetic Has associated chemicals Has associated genes Has associated exposure references Vohwinkel Syndrome, Variant Form Has associated chemicals Has associated genes

Top ↑ Descendants

None.