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DO Term : hereditary spastic paraplegia 12 [DOID:0110765] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.
  • synonyms:
  • GARD:9586,
  • OMIM:604805,
  • autosomal dominant spastic paraplegia type 12,
  • ORDO:100993,
  • 604805,
  • SPG12,
  • ICD10CM:G11.4,
  • autosomal dominant spastic paraplegia 12
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Disease

Diseases --> Human genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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