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Echinobase
Summary Literature (0)
DOID:0110818 - hereditary spastic paraplegia 73

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the CPT1C gene on chromosome 19q13.

Synonyms: SPG73, autosomal dominant spastic paraplegia 73, autosomal dominant spastic paraplegia type 73,

Echinobase Genes :



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)