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 28 ID (Ontology) DOID:0110779 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22.
Also Known As "autosomal recessive spastic paraplegia 28" ; "autosomal recessive spastic paraplegia type 28" ; "SPG28"
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 28
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Is a autosomal recessive disease
hereditary spastic paraplegia
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Synonyms
  • "autosomal recessive spastic paraplegia 28" EXACT
    "autosomal recessive spastic paraplegia type 28" EXACT
    "SPG28" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:609340
ORDO:101008