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amelogenesis imperfecta type 1A

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Any amelogenesis imperfecta in which the cause of the disease is a mutation in the LAMB3 gene.
Uniprot Description A form of amelogenesis imperfecta, a disorder characterized by defective enamel formation. The enamel may be hypoplastic, hypomineralized or both, and affected teeth may be discoloured, sensitive or prone to disintegration.
Mondo Term and Equivalent IDs
MONDO:0007094:  amelogenesis imperfecta type 1A
GARD:0000645: 
MESH:C538240: