DISEASES - autosomal dominant cutis laxa 2

Human genes for autosomal dominant cutis laxa 2

Autosomal dominant cutis laxa 2 [DOID:0070136]

An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutation in the FBLN5 gene on chromosome 14q32.

Synonyms: autosomal dominant cutis laxa 2, DOID:0070136, ADCL2

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.