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DO Term : hereditary spastic paraplegia 56 [DOID:0110808] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25.
  • synonyms:
  • 615030,
  • SPG56,
  • ICD10CM:G11.4,
  • autosomal recessive spastic paraplegia type 56,
  • OMIM:615030,
  • autosomal recessive spastic paraplegia 56,
  • ORDO:320411
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Disease

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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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