|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Aplasia of the lacrimal and salivary glands (ALSG) is a rare autosomal dominant disorder characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying features since infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation. (Orphanet Rare Disease Ontology, Orphanet_86815)|
|Downloads & Tools|
1 genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset.
|FGF10||fibroblast growth factor 10||2.88009|