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DO Term : autosomal recessive spinocerebellar ataxia 11 [DOID:0080063] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32.
  • synonyms:
  • SCAR11,
  • OMIM:614229,
  • 614229
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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