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DOID:0110787 - hereditary spastic paraplegia 36
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.
Synonyms: SPG36, autosomal dominant spastic paraplegia 36, autosomal dominant spastic paraplegia type 36,
Xenbase Genes :
MONDO:0013132 - hereditary spastic paraplegia 36 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee