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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 : vps37a
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