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Human Disease

hereditary spastic paraplegia 30

Term ID
DOID:0110781
Synonyms
  • autosomal dominant spastic paraplegia 30
  • autosomal recessive spastic paraplegia 30
  • autosomal spastic paraplegia type 30
  • SPG30
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37. (2)
References
Ontology
Human Disease   ( DOID:0110781 )
Relationships
is a type of
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Genes Involved
Zebrafish Models