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 10 ID (Ontology) DOID:0110763 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13.
Also Known As "autosomal dominant spastic paraplegia 10" ; "autosomal dominant spastic paraplegia type 10" ; "SPG10"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 hereditary spastic paraplegia 10       1      1
 for disease ribbon | hereditary spastic paraplegia 10       1       --
 model of | hereditary spastic paraplegia 10       1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 10  2 rec.
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Is a autosomal dominant disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "autosomal dominant spastic paraplegia 10" EXACT
    "autosomal dominant spastic paraplegia type 10" EXACT
    "SPG10" EXACT OMO:0003012
Secondary IDs
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GARD:9590
ICD10CM:G11.4
MIM:604187
ORDO:100991