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DO Term : hereditary spastic paraplegia 6 [DOID:0110811] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.
  • synonyms:
  • autosomal dominant familial spastic paraplegia type 3,
  • OMIM:600363,
  • SPG6,
  • autosomal dominant spastic paraplegia 6,
  • FSP3,
  • 600363,
  • ORDO:100988,
  • ICD10CM:G11.4,
  • autosomal dominant spastic paraplegia type 6
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Disease

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Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents