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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

Referenced OMIM:
OMIM:312920 - SPASTIC PARAPLEGIA 2, X-LINKED; SPG2

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : plp1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary spastic paraplegia (is_a)


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