Showing entry for Muscular Dystrophy, Oculopharyngeal
| General Disease Information | |
|---|---|
| BXGD Id | BXGD006139 |
| Disease Name | Muscular Dystrophy, Oculopharyngeal |
| Disease CUI Id | C0270952 |
| MeSH Codes | C16 C05 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations
|