hereditary spastic paraplegia 77

Summary

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: autosomal recessive spastic paraplegia 77, SPG77

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 - distal epiphysis of distal phalanx of manual digit 2

MONDO:0014882 - distal epiphysis of distal phalanx of manual digit 2

MIM:

MIM:617046 - SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE; SPG77

MIM:617046 - SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE; SPG77

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)