Summary Literature (0)

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

Xenbase Genes : entpd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014303 - hereditary spastic paraplegia 64

MIM:

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