amelogenesis imperfecta type 1A

Summary
Synonym
  • AI1A
  • amelogenesis imperfecta hypoplastic type IA
  • amelogenesis imperfecta type IA
Definition
An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.
Super Class
amelogenesis imperfecta autosomal dominant disease
Disease Ontology
DOID:0110054
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3914 LAMB3 laminin subunit beta 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
16780 Lamb3 laminin, beta 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
177292 lam-1 Laminin subunit beta-1

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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