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 18 ID (Ontology) DOID:0110771 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.
Also Known As "SPG18"
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  paraplegia
   |__hereditary spastic paraplegia
       |__hereditary spastic paraplegia 18
           |__hereditary spastic paraplegia 18A
           |__hereditary spastic paraplegia 18B
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Is a hereditary spastic paraplegia
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Synonyms
  • "SPG18" EXACT OMO:0003012
Secondary IDs
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GARD:4922
ICD10CM:G11.4
ORDO:209951