amelogenesis imperfecta type 2A1

Summary
Synonym
  • AI2A1
  • amelogenesis imperfecta pigmented hypomaturation type 1
  • amelogenesis imperfecta type IIA1
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13.
Super Class
amelogenesis imperfecta autosomal recessive disease
Disease Ontology
DOID:0110057
Mondo Disease Ontology
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9622 KLK4 kallikrein related peptidase 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
56640 Klk4 kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024