Showing entry for Spinocerebellar tract degeneration
| General Disease Information | |
|---|---|
| BXGD Id | BXGD016422 |
| Disease Name | Spinocerebellar tract degeneration |
| Disease CUI Id | C1866751 |
| MeSH Codes | C16 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0000707 |
| Human Phenotype Ontology Term | Abnormality of the nervous system |
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| Disorder Network | disorder-protein-compound-food associations |
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