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DO Term : hereditary spastic paraplegia 38 [DOID:0110789] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.
  • synonyms:
  • SPG38,
  • 612335,
  • autosomal dominant spastic paraplegia type 38,
  • autosomal dominant spastic paraplegia 38,
  • ORDO:171617,
  • ICD10CM:G11.4,
  • OMIM:612335
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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