Showing entry for Osteogenesis imperfecta, type 5
| General Disease Information | |
|---|---|
| BXGD Id | BXGD017956 |
| Disease Name | Osteogenesis imperfecta, type 5 |
| Disease CUI Id | C2931093 |
| MeSH Codes | C16 C17 C05 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|