Summary Literature (0)

DOID:0110771 - hereditary spastic paraplegia 18

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.

Synonyms: IDMDC, SPG18, autosomal recessive spastic paraplegia 18, autosomal recessive spastic paraplegia type 18, intellectual disability, motor dysfunction and joint contractures,

Echinobase Genes : LOC592559


OMIM:

OMIM:611225 - spastic paraplegia 18, autosomal recessive; spg18

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee