hereditary spastic paraplegia 57

Summary

DOID:0110809 - hereditary spastic paraplegia 57

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the TFG gene on chromosome 3q12.

Synonyms: autosomal recessive spastic paraplegia 57, autosomal recessive spastic paraplegia type 57, SPG57

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

: tfg

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014295 - hereditary spastic paraplegia 57

MONDO:0014295 - hereditary spastic paraplegia 57

MIM:

MIM:615658 - SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57

MIM:615658 - SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57

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)