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DO Term : hereditary spastic paraplegia 25 [DOID:0110776] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 6q23-q24.1.
  • synonyms:
  • ICD10CM:G11.4,
  • GARD:9582,
  • autosomal recessive spastic paraplegia 25,
  • OMIM:608220,
  • autosomal recessive spastic paraplegia type 25,
  • 608220,
  • ORDO:101005,
  • SPG25
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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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