Amelogenesis Imperfecta Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A dental enamel hypoplasia characterized by abnormal enamel formation. (Human Disease Ontology, DOID_2187)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000567
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Genes

2 genes/proteins associated with the disease Amelogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FAM83H family with sequence similarity 83, member H 2.88009
ENAM enamelin 2.88009