Term Name: hereditary spastic paraplegia 30
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.
Ontology: Human Disease [DOID:0110781]   ( DOID:0110781 )

Relationships
is a type of: autosomal genetic disease hereditary spastic paraplegia