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DOID:0110774 - hereditary spastic paraplegia 23
Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.
Synonyms: Lison syndrome, Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome, spastic paraplegia 23, spastic paraplegia with pigmentary abnormalities, SPG23
Xenbase Genes
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Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010046 - hereditary spastic paraplegia 23 |
MIM:
MIM:270750 - SPASTIC PARAPLEGIA 23, AUTOSOMAL RECESSIVE; SPG23 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee