Summary Literature (0)

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

Echinobase Genes : spg7


OMIM:

MIM:607259 - spastic paraplegia 7, autosomal recessive; spg7

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee