DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary spastic paraplegia 72

Hereditary spastic paraplegia 72 [DOID:0110817]

A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP2 gene on chromosome 5q31.

Synonyms:  hereditary spastic paraplegia 72,  DOID:0110817,  familial spastic paraplegia 72,  autosomal spastic paraplegia type 72,  SPG72

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.