Showing entry for Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
| General Disease Information | |
|---|---|
| BXGD Id | BXGD013967 |
| Disease Name | Myopathy, Actin, Congenital, with Excess of Thin Myofilaments |
| Disease CUI Id | C1834339 |
| MeSH Codes | C05 C10 |
| Disease Class Name | Musculoskeletal Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 DOID:225 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity; syndrome |
| Disorder Network | disorder-protein-compound-food associations
|