hereditary spastic paraplegia 55

Summary

DOID:0110807 - hereditary spastic paraplegia 55

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24.

Synonyms: SPG55, autosomal recessive spastic paraplegia 55, autosomal recessive spastic paraplegia type 55,

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

: mtrfr

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014020 - hereditary spastic paraplegia 55

MONDO:0014020 - hereditary spastic paraplegia 55

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

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

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