hereditary spastic paraplegia 7

Summary

DOID:0110816 - hereditary spastic paraplegia 7

Disease Ontology Definition:A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24.

Synonyms: autosomal recessive spastic paraplegia 7, spastic paraplegia type 7, SPG7

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

: spg7

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011803 - hereditary spastic paraplegia 7

MONDO:0011803 - hereditary spastic paraplegia 7

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)