FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary spastic paraplegia 23 ID (Ontology) DOID:0110774 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.
Also Known As "Lison syndrome" ; "Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome" ; "spastic paraplegia 23" (for all, see Synonyms field below)
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 23
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Is a autosomal recessive disease
hereditary spastic paraplegia
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Synonyms
  • "Lison syndrome" EXACT
    "Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome" EXACT
    "spastic paraplegia 23" EXACT
    "spastic paraplegia with pigmentary abnormalities" EXACT
    "SPG23" EXACT OMO:0003012
Secondary IDs
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GARD:336
ICD10CM:G11.4
MIM:270750
ORDO:101003