Lacrimoauriculodentodigital syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538132
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Genes

3 genes/proteins associated with the disease Lacrimoauriculodentodigital syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FGF10 fibroblast growth factor 10 2.88009
FGFR2 fibroblast growth factor receptor 2 2.88009
FGFR3 fibroblast growth factor receptor 3 2.88009