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Disease Ruvalcaba Churesigaew Myhre syndrome

Name Ruvalcaba Churesigaew Myhre syndrome
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C537190

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 Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Progeria Has associated chemicals Has associated genes Ruvalcaba Churesigaew Myhre syndrome
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Progeria Has associated chemicals Has associated genes Ruvalcaba Churesigaew Myhre syndrome

Top ↑ Descendants

None.