Showing entry for MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
| General Disease Information | |
|---|---|
| BXGD Id | BXGD013832 |
| Disease Name | MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED |
| Disease CUI Id | C1832370 |
| MeSH Codes | C16 C05 C10 C14 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular 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
|