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DO Term : hereditary spastic paraplegia 26 [DOID:0110777] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13.
  • synonyms:
  • GARD:9587,
  • autosomal recessive spastic paraplegia type 26,
  • autosomal recessive spastic paraplegia 26,
  • SPG26,
  • ORDO:101006,
  • OMIM:609195,
  • ICD10CM:G11.4,
  • 609195,
  • GM2 synthase deficiency
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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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