hereditary spastic paraplegia 61

Summary

DOID:0110812 - hereditary spastic paraplegia 61

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12.

Synonyms: SPG61, autosomal recessive spastic paraplegia 61, autosomal recessive spastic paraplegia type 61,

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

: arl6ip1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014304 - hereditary spastic paraplegia 61

MONDO:0014304 - hereditary spastic paraplegia 61

Other Model Organisms: AGR, 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)