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DO Term : hereditary spastic paraplegia 41 [DOID:0110793] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.
  • synonyms:
  • SPG41,
  • autosomal dominant spastic paraplegia 41,
  • ICD10CM:G11.4,
  • OMIM:613364,
  • 613364,
  • autosomal dominant spastic paraplegia type 41,
  • ORDO:320355
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