hereditary spastic paraplegia 33

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Summary

Literature (0)

DOID:0110784 - hereditary spastic paraplegia 33

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE27 gene on chromosome 10q24.

Synonyms: autosomal dominant spastic paraplegia 33, SPG33

Xenbase 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

: zfyve27

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012448 - hereditary spastic paraplegia 33

MONDO:0012448 - hereditary spastic paraplegia 33

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

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

Parent(s): autosomal dominant disease (is_a), hereditary spastic paraplegia (is_a)