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 9B ID (Ontology) DOID:0110825 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24.
Also Known As "autosomal recessive complex spastic paraplegia type 9B" ; "autosomal recessive spastic paraplegia 9B" ; "SPG9B"
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 Genes
 hereditary spastic paraplegia 9B       1
 for disease ribbon | hereditary spastic paraplegia 9B       1
 model of | hereditary spastic paraplegia 9B       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 9B  1 rec.
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Is a autosomal recessive disease
hereditary spastic paraplegia
Part of
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Synonyms
  • "autosomal recessive complex spastic paraplegia type 9B" EXACT
    "autosomal recessive spastic paraplegia 9B" EXACT
    "SPG9B" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:616586
ORDO:447760