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amelogenesis imperfecta type 2A1

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


GARD Rare
Mondo Description Any amelogenesis imperfecta in which the cause of the disease is a mutation in the KLK4 gene.
Uniprot Description A defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel.
Mondo Term and Equivalent IDs
MONDO:0008772:  amelogenesis imperfecta type 2A1
GARD:0009495: 
MESH:C538242: 
MESH:C567146: