hereditary spastic paraplegia 23

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Summary

Literature (0)

DOID:0110774 - hereditary spastic paraplegia 23

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.

Synonyms: Lison syndrome, SPG23, Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome, spastic paraplegia 23, spastic paraplegia with pigmentary abnormalities,

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)