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DO Term : hereditary spastic paraplegia 75 [DOID:0110820] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.
  • synonyms:
  • ORDO:459056,
  • autosomal recessive spastic paraplegia type 75,
  • OMIM:616680,
  • 616680,
  • autosomal recessive spastic paraplegia 75,
  • ICD10CM:G11.4,
  • SPG75
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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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