Term Name:	hereditary spastic paraplegia 87
Synonyms:	autosomal recessive spastic paraplegia 87, SPG87
Definition:	A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3.
Ontology:	Human Disease [DOID:0070456]   ( DOID:0070456 )