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DO Term : hereditary spastic paraplegia 31 [DOID:0110782] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.
  • synonyms:
  • SPG31,
  • GARD:10817,
  • ICD10CM:G11.4,
  • ORDO:101011,
  • OMIM:610250,
  • autosomal dominant spastic paraplegia type 31,
  • autosomal dominant spastic paraplegia 31,
  • 610250
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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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