DISEASES

Disease-gene associations mined from literature

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Human genes for platelet-type bleeding disorder 11

Platelet-type bleeding disorder 11 [DOID:0111057]

A blood platelet disease characterized by autosomal recessive inheritance of mild to moderate bleeding and defective platelet activation and aggregation in response to collagen that has_material_basis_in compound heterozygous mutation in the GP6 gene on chromosome 19q13.

Synonyms:  platelet-type bleeding disorder 11,  DOID:0111057,  platelettype bleeding disorder 11,  BDPLT11,  glycoprotein VI deficiency ...

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.