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Echinobase
Summary Literature (0)
DOID:0110773 - hereditary spastic paraplegia 2

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.

Synonyms: SPG2, X-linked spastic paraplegia 2, spastic paraplegia type 2,

Echinobase Genes :


OMIM:
MIM:312920 - spastic paraplegia 2, x-linked; spg2

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

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