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Disease Craniodiaphyseal Dysplasia, Autosomal Dominant

Name Craniodiaphyseal Dysplasia, Autosomal Dominant
Categories Congenital abnormality | Genetic disease (inborn) | Musculoskeletal disease
MeSH® ID C567275

Top ↑ Ancestors

1. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases, Developmental Has associated chemicals Has associated genes Osteochondrodysplasias Has associated chemicals Has associated genes Craniodiaphyseal Dysplasia, Autosomal Dominant
2. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Musculoskeletal Abnormalities Has associated chemicals Has associated genes Has associated exposure references Craniofacial Abnormalities Has associated chemicals Has associated genes Has associated exposure references Craniodiaphyseal Dysplasia, Autosomal Dominant
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated exposure references Musculoskeletal Abnormalities Has associated chemicals Has associated genes Has associated exposure references Craniofacial Abnormalities Has associated chemicals Has associated genes Has associated exposure references Craniodiaphyseal Dysplasia, Autosomal Dominant
4. 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 Osteochondrodysplasias Has associated chemicals Has associated genes Craniodiaphyseal Dysplasia, Autosomal Dominant

Top ↑ Descendants

None.