Transient bullous dermolysis of the newborn Gene Set

Dataset CTD 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 http://ctdbase.org/detail.go?type=disease&acc=MESH:C536979
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Genes

1 genes/proteins associated with the disease Transient bullous dermolysis of the newborn from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
COL7A1 collagen, type VII, alpha 1 2.88009