Term Name: hereditary spastic paraplegia 77
Synonyms: autosomal recessive spastic paraplegia 77, SPG77
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25.
Ontology: Human Disease [DOID:0110822]   ( DOID:0110822 )

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