DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for transient bullous dermolysis of the newborn

Transient bullous dermolysis of the newborn [DOID:0111345]

An epidermolysis bullosa dystrophica characterized by generalized blistering at birth that usually regresses by 6 to 24 months of age that has_material_basis_in heterozygous, compound heterozygous or homozygous mutation in COL7A1 on chromosome 3p21.31.

Synonyms:  transient bullous dermolysis of the newborn,  DOID:0111345,  transient bullous dermolysis of the newborns,  DEB-BDN,  DEB, bullous dermolysis of the newborn ...

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.