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 49 ID (Ontology) DOID:0110801 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.
Also Known As "autosomal recessive spastic paraplegia 49" ; "autosomal recessive spastic paraplegia type 49" ; "SPG49"
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 Genes
 hereditary spastic paraplegia 49       1
 for disease ribbon | hereditary spastic paraplegia 49       1
 model of | hereditary spastic paraplegia 49       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 49  1 rec.
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Is a autosomal recessive disease
hereditary spastic paraplegia
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Synonyms
  • "autosomal recessive spastic paraplegia 49" EXACT
    "autosomal recessive spastic paraplegia type 49" EXACT
    "SPG49" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:615031
ORDO:320385