DISEASES

Disease-gene associations mined from literature

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Human genes for CST3-related cerebral amyloid angiopathy

CST3-related cerebral amyloid angiopathy [DOID:0070027]

A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of CST3 on chromosome 20p11.21.

Synonyms:  CST3-related cerebral amyloid angiopathy,  CST3related cerebral amyloid angiopathy,  DOID:0070027,  Hereditary Cerebral Amyloid Angiopathy, Icelandic Type,  Amyloidosis, Cerebroarterial, Icelandic Type ...

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.