Showing entry for Flatfoot
| General Disease Information | |
|---|---|
| BXGD Id | BXGD001050 |
| Disease Name | Flatfoot |
| Disease CUI Id | C0016202 |
| MeSH Codes | C16 C05 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| Semantic Type | Anatomical Abnormality |
| Human Phenotype Ontology Id | HP:0040064 |
| Human Phenotype Ontology Term | Abnormality of limbs |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|