hereditary spastic paraplegia 77

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Summary

Literature (0)

DOID:0110822 - hereditary spastic paraplegia 77

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25.

Synonyms: SPG77, autosomal recessive spastic paraplegia 77,

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

: fars2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014882 - hereditary spastic paraplegia 77

MONDO:0014882 - hereditary spastic paraplegia 77

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)