|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Laryngo onycho cutaneous syndrome from the curated CTD Gene-Disease Associations dataset.
|LAMA3||laminin, alpha 3||2.88009|