hereditary spastic paraplegia 53

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Summary

Literature (0)

DOID:0110805 - hereditary spastic paraplegia 53

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22.

Synonyms: SPG53, autosomal recessive spastic paraplegia 53, autosomal recessive spastic paraplegia type 53,

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

: vps37a

OMIM:

MIM:614898 - spastic paraplegia 53, autosomal recessive; spg53

MIM:614898 - spastic paraplegia 53, autosomal recessive; spg53

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

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

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