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DOID:0110765 - hereditary spastic paraplegia 12
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.
Synonyms: SPG12, autosomal dominant spastic paraplegia 12, autosomal dominant spastic paraplegia type 12,
Xenbase Genes : rtn2
MONDO:0011489 - hereditary spastic paraplegia 12 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee