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DO Term : autosomal recessive spinocerebellar ataxia 22 [DOID:0111614] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2.
  • synonyms:
  • SCAR22,
  • OMIM:616948,
  • 616948
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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