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 89 ID (Ontology) DOID:0070458 (Human Disease)
Definition A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.
Also Known As "autosomal recessive spastic paraplegia 89" ; "SPG89"
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 Genes
 hereditary spastic paraplegia 89       3
 for disease ribbon | hereditary spastic paraplegia 89       3
 model of | hereditary spastic paraplegia 89       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease____
paraplegia                         |
 |__hereditary spastic paraplegia__|
                                   hereditary spastic paraplegia 89  3 rec.
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Is a autosomal recessive disease
hereditary spastic paraplegia
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Synonyms
  • "autosomal recessive spastic paraplegia 89" EXACT
    "SPG89" EXACT OMO:0003012
Secondary IDs
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MIM:620379