Transient Bullous Dermolysis Of The Newborn Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Transient bullous dermolysis of the newborn is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life. (Orphanet Rare Disease Ontology, Orphanet_79411)
External Link https://www.disgenet.org/browser/0/1/0/C1851573
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Genes

1 genes associated with the disease Transient Bullous Dermolysis Of The Newborn in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COL7A1 collagen, type VII, alpha 1