Term Name: hereditary spastic paraplegia 64
Synonyms: autosomal recessive spastic paraplegia 64, autosomal recessive spastic paraplegia type 64, SPG64
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.
Ontology: Human Disease [DOID:0110815]   ( DOID:0110815 )

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