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 42 ID (Ontology) DOID:0110794 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.
Also Known As "autosomal dominant spastic paraplegia 42" ; "autosomal dominant spastic paraplegia type 42" ; "SPG42"
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 Genes
 hereditary spastic paraplegia 42       1
 for disease ribbon | hereditary spastic paraplegia 42       1
 model of | hereditary spastic paraplegia 42       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 42  1 rec.
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Is a autosomal dominant disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "autosomal dominant spastic paraplegia 42" EXACT
    "autosomal dominant spastic paraplegia type 42" EXACT
    "SPG42" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:612539
ORDO:171863