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 30B ID (Ontology) DOID:0070646 (Human Disease)
Definition A hereditary spastic paraplegia 30 that has_material_basis_in homozygous mutation in the KIF1A gene on chromosome 2q37.
Also Known As "autosomal recessive spastic paraplegia 30"
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 Genes
 hereditary spastic paraplegia 30B       1
 for disease ribbon | hereditary spastic paraplegia 30B       1
 model of | hereditary spastic paraplegia 30B       1
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autosomal genetic disease
 |__autosomal recessive disease_______
 |__hereditary spastic paraplegia 30__|
hereditary spastic paraplegia         |
 |__hereditary spastic paraplegia 30__|
                                      hereditary spastic paraplegia 30B  1 rec.
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Is a autosomal recessive disease
hereditary spastic paraplegia 30
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Synonyms
  • "autosomal recessive spastic paraplegia 30" EXACT
Secondary IDs
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MIM:620607