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DOID:0110772 - hereditary spastic paraplegia 19
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q.
Synonyms: SPG19, autosomal dominant spastic paraplegia 19, autosomal dominant spastic paraplegia type 19,
Xenbase Genes :
MONDO:0011785 - hereditary spastic paraplegia 19 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee