Showing entry for Osteogenesis imperfecta, type 1A
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005912 |
| Disease Name | Osteogenesis imperfecta, type 1A |
| Disease CUI Id | C0268357 |
| MeSH Codes | C16 C17 C05 C07 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|