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Summary Literature (0)
DOID:0070456 - hereditary spastic paraplegia 87


Disease Ontology 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.

Synonyms: SPG87, autosomal recessive spastic paraplegia 87,

Xenbase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), hereditary spastic paraplegia (is_a)