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DO Term : hereditary spastic paraplegia 7 [DOID:0110816] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24.
  • synonyms:
  • 607259,
  • SPG7,
  • autosomal recessive spastic paraplegia 7,
  • spastic paraplegia type 7,
  • ICD10CM:G11.4,
  • OMIM:607259,
  • ORDO:99013
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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