DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for platelet-type bleeding disorder 3

Platelet-type bleeding disorder 3 [DOID:0111056]

A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2.

Synonyms:  platelet-type bleeding disorder 3,  DOID:0111056,  platelettype bleeding disorder 3,  BDPLT3,  platelet type-von Willebrand disease ...

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.