DISEASES

Disease-gene associations mined from literature

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Human genes for osteogenesis imperfecta type 6

Osteogenesis imperfecta type 6 [DOID:0110350]

An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINF1 gene on chromosome 17p13.3.

Synonyms:  osteogenesis imperfecta type 6,  DOID:0110350,  OI6,  osteogenesis imperfecta type VI,  osteogenesis imperfecta type VIs

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.