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amelogenesis imperfecta type 1C

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive defect of dental enamel formation. Teeth show local hypoplastic and unmineralized enamel, and a yellow-brown discoloration. Enamel defects can be associated with facial and oral features including vertical dysgnathia and anterior openbite malocclusion.
Mondo Term and Equivalent IDs
MONDO:0008770:  amelogenesis imperfecta type 1C
MESH:C567147: 
UMLS:C2673923: