Term Name: hereditary spastic paraplegia 72A
Synonyms: autosomal spastic paraplegia type 72, SPG72
Definition: A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2.
Ontology: Human Disease [DOID:0110817]   ( DOID:0110817 )

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