hereditary spastic paraplegia 16

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Summary

Literature (0)

DOID:0110769 - hereditary spastic paraplegia 16

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.

Synonyms: SPG16, X-linked spastic paraplegia 16, X-linked spastic paraplegia type 16,

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): hereditary spastic paraplegia (is_a)