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DO Term : hereditary spastic paraplegia 46 [DOID:0110798] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.
  • synonyms:
  • autosomal recessive spastic paraplegia type 46,
  • SPG46,
  • OMIM:614409,
  • autosomal recessive spastic paraplegia 46,
  • 614409,
  • ORDO:320391,
  • ICD10CM:G11.4
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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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