hereditary spastic paraplegia 12

Summary

DOID:0110765 - hereditary spastic paraplegia 12

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.

Synonyms: autosomal dominant spastic paraplegia 12, autosomal dominant spastic paraplegia type 12, SPG12

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rtn2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011489 - hereditary spastic paraplegia 12

MONDO:0011489 - hereditary spastic paraplegia 12

MIM:

MIM:604805 - SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12

MIM:604805 - SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12

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

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

Parent(s): autosomal dominant disease (is_a), hereditary spastic paraplegia (is_a)