hereditary spastic paraplegia 29

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Summary

Literature (0)

DOID:0110780 - hereditary spastic paraplegia 29

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1.

Synonyms: SPG29, autosomal dominant spastic paraplegia 29,

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

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012334 - hereditary spastic paraplegia 29

MONDO:0012334 - hereditary spastic paraplegia 29

Other Model Organisms: AGR, 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)