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DO Term : hereditary spastic paraplegia 34 [DOID:0110785] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq24-q25.
  • synonyms:
  • OMIM:300750,
  • ICD10CM:G11.4,
  • 300750,
  • X-linked spastic paraplegia 34,
  • SPG34,
  • X-linked spastic paraplegia type 34,
  • ORDO:171607
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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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