DISEASES - autosomal dominant Alport syndrome

Human genes for autosomal dominant Alport syndrome

Autosomal dominant Alport syndrome [DOID:0110032]

An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene.

Synonyms: autosomal dominant Alport syndrome, autosomal dominant Alport disease, autosomal dominant Alport disorder, autosomal dominant Alport syndromes, DOID:0110032

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.