DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for hereditary spastic paraplegia 11

Hereditary spastic paraplegia 11 [DOID:0110764]

A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.

Synonyms:  hereditary spastic paraplegia 11,  DOID:0110764,  familial spastic paraplegia 11,  autosomal recessive spastic paraplegia 11,  autosomal recessive spastic paraplegia complicated with thin corpus callosum ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.