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Disease Osteogenesis imperfecta, Levin type

Name Osteogenesis imperfecta, Levin type
Synonyms Gnathodiaphyseal Dysplasia | Gnathodiaphyseal Sclerosis | Levin syndrome 2 | Osteogenesis imperfecta with unusual skeletal lesions
Categories Connective tissue disease | Genetic disease (inborn) | Musculoskeletal disease
MeSH® ID C536039

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 Osteogenesis Imperfecta Has associated chemicals Has associated genes Osteogenesis imperfecta, Levin type
2. 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 Osteogenesis Imperfecta Has associated chemicals Has associated genes Osteogenesis imperfecta, Levin type
3. DiseasesSkin and Connective Tissue Diseases Has associated chemicals Has associated genes Has associated exposure references Connective Tissue Diseases Has associated chemicals Has associated genes Has associated exposure references Collagen Diseases Has associated chemicals Has associated genes Osteogenesis Imperfecta Has associated chemicals Has associated genes Osteogenesis imperfecta, Levin type

Top ↑ Descendants

None.