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Disease Ontology Browser
hereditary spastic paraplegia 23 (DOID:0110774)
Alliance: disease page
Synonyms: Lison syndrome; Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome; spastic paraplegia 23; spastic paraplegia with pigmentary abnormalities; SPG23
Alt IDs: OMIM:270750, ICD10CM:G11.4, ORDO:101003
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory