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 13 ID (Ontology) DOID:0110766 (Human Disease)
Definition A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33.
Also Known As "autosomal dominant spastic paraplegia 13" ; "SPG13"
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 Genes
 hereditary spastic paraplegia 13       4
 for disease ribbon | hereditary spastic paraplegia 13       4
 model of | hereditary spastic paraplegia 13       4
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 13  4 rec.
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Is a autosomal dominant disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "autosomal dominant spastic paraplegia 13" EXACT
    "SPG13" EXACT OMO:0003012
Secondary IDs
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GARD:9616
ICD10CM:G11.4
MIM:605280
ORDO:100994