Summary Literature (0)

DOID:0110764 - hereditary spastic paraplegia 11

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.

Synonyms: autosomal recessive spastic paraplegia 11, autosomal recessive spastic paraplegia complicated with thin corpus callosum, autosomal recessive spastic paraplegia type 11, autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum, HSP-TCC, Nakamura-Osame syndrome, spastic paraplegia-intellectual disability-thin corpus callosum syndrome, SPG11

Xenbase Genes : spg11

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011445 - hereditary spastic paraplegia 11

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

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