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DOID:0110776 - hereditary spastic paraplegia 25
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 6q23-q24.1.
Synonyms: SPG25, autosomal recessive spastic paraplegia 25, autosomal recessive spastic paraplegia type 25,
Xenbase Genes :
MONDO:0011992 - hereditary spastic paraplegia 25 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee