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 43 ID (Ontology) DOID:0110795 (Human Disease)
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the C19ORF12 gene on chromosome 19q12.
Also Known As "autosomal recessive spastic paraplegia 43" ; "autosomal recessive spastic paraplegia type 43" ; "SPG43"
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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 43       2      1
 for disease ribbon | hereditary spastic paraplegia 43       2       --
 model of | hereditary spastic paraplegia 43       2       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 43  3 rec.
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Is a autosomal recessive disease
hereditary spastic paraplegia
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Synonyms
  • "autosomal recessive spastic paraplegia 43" EXACT
    "autosomal recessive spastic paraplegia type 43" EXACT
    "SPG43" EXACT OMO:0003012
Secondary IDs
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ICD10CM:G11.4
MIM:615043
ORDO:320370