hereditary spastic paraplegia 64

Summary

DOID:0110815 - hereditary spastic paraplegia 64

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.

Synonyms: autosomal recessive spastic paraplegia 64, autosomal recessive spastic paraplegia type 64, SPG64

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

: entpd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014303 - hereditary spastic paraplegia 64

MONDO:0014303 - hereditary spastic paraplegia 64

MIM:

MIM:615683 - SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64

MIM:615683 - SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64

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)