hereditary spastic paraplegia 38

Summary

DOID:0110789 - hereditary spastic paraplegia 38

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 4p16-p15.

Synonyms: SPG38, autosomal dominant spastic paraplegia 38, autosomal dominant spastic paraplegia type 38,

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:0012867 - hereditary spastic paraplegia 38

MONDO:0012867 - hereditary spastic paraplegia 38

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)