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DO Term : hereditary spastic paraplegia 16 [DOID:0110769] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.
  • synonyms:
  • ORDO:100997,
  • OMIM:300266,
  • 300266,
  • X-linked spastic paraplegia type 16,
  • X-linked spastic paraplegia 16,
  • GARD:9585,
  • ICD10CM:G11.4,
  • SPG16
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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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