| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormality of the spinocerebellar tracts, a set of axonal fibers originating in the spinal cord and terminating in the ipsilateral cerebellum. The spinocerebellar tract convey information to the cerebellum about limb and joint position (proprioception). They comprise the ventral spinocerebellar tract (FMA:72642), the anterior spinocerebellar tract (FMA:72642), and the posterior spinocerebellar tract (FMA:72641). (Human Phenotype Ontology, HP_0003133) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003133 |
| Similar Terms | |
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6 genes associated with the abnormality of the spinocerebellar tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
