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Human Disease

spastic ataxia 2

Term ID
DOID:0050941
Synonyms
Definition
A spastic ataxia that is characterized by cerebellar ataxia, spasticity and peripheral neuropathy in the first two decades of life, has_material_basis_in homozygous mutation in the KIF1C gene on chromosome 17p13. https://www.ncbi.nlm.nih.gov/pubmed/17273843
References
Ontology
Human Disease   ( DOID:0050941 )
Relationships
is a type of
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Genes Involved
Zebrafish Models