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Metadata
ID	DOID:0050944
Name	spastic ataxia 5
Definition	A spastic ataxia that is characterized by early onset of cerebellar ataxia, spasticity, oculomotor apraxia, dystonia and myoclonic epilepsy, has_material_basis_in homozygous mutation in the AFG3L2 gene on chromosome 18p11. https://www.ncbi.nlm.nih.gov/pubmed/22022284
Xrefs	MIM:614487
Parent Relationships	is_a spastic ataxia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance