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DO Term : hereditary spastic paraplegia 48 [DOID:0110800] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.
  • synonyms:
  • autosomal recessive spastic paraplegia 48,
  • ORDO:306511,
  • autosomal recessive spastic paraplegia type 48,
  • ICD10CM:G11.4,
  • 613647,
  • SPG48,
  • OMIM:613647
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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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