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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,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014568 - hereditary spastic paraplegia 73 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee