hereditary spastic paraplegia 62

Summary

DOID:0110813 - hereditary spastic paraplegia 62

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN1 gene on chromosome 10q24.

Synonyms: autosomal recessive spastic paraplegia 62, autosomal recessive spastic paraplegia type 62, SPG62

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

: erlin1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014302 - hereditary spastic paraplegia 62

MONDO:0014302 - hereditary spastic paraplegia 62

MIM:

MIM:615681 - SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE; SPG62

MIM:615681 - SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE; SPG62

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)