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 19 ID (Ontology) DOID:0110772 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 9q.
Also Known As "autosomal dominant spastic paraplegia 19" ; "autosomal dominant spastic paraplegia type 19" ; "SPG19"
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 19
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Is a autosomal dominant disease
hereditary spastic paraplegia
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Synonyms
  • "autosomal dominant spastic paraplegia 19" EXACT
    "autosomal dominant spastic paraplegia type 19" EXACT
    "SPG19" EXACT OMO:0003012
Secondary IDs
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GARD:9588
ICD10CM:G11.4
MIM:607152
ORDO:100999