Laryngo onycho cutaneous syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description LOC syndrome is a subtype of junctional epidermolysis bullosa (JEB, see this term) characterized by an altered cry in the neonatal period and by aberrant production of granulation tissue in particular affecting the upper airway tract, conjunctiva and periungual/subungual sites. (Orphanet Rare Disease Ontology, Orphanet_2407)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537032
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Laryngo onycho cutaneous syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LAMA3 laminin, alpha 3 2.88009