Showing entry for Striatonigral Degeneration, Infantile, Mitochondrial
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014352 |
| Disease Name | Striatonigral Degeneration, Infantile, Mitochondrial |
| Disease CUI Id | C1839022 |
| MeSH Codes | C10 |
| Disease Class Name | 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
|