| 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 |
| Similar Terms | |
| Downloads & Tools |
2 genes/proteins associated with the disease Amelogenesis Imperfecta from the curated CTD Gene-Disease Associations dataset.
