Term Name: hereditary spastic paraplegia 55
Synonyms: autosomal recessive spastic paraplegia 55, autosomal recessive spastic paraplegia type 55, SPG55
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24.
Ontology: Human Disease [DOID:0110807]   ( DOID:0110807 )

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