|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes. (Human Disease Ontology, DOID_0050331)|
|Downloads & Tools|
3 genes/proteins associated with the disease Lacrimoauriculodentodigital syndrome from the curated CTD Gene-Disease Associations dataset.