amelogenesis imperfecta hypomaturation type 2A2

Summary
Synonym
  • AI2A2
  • amelogenesis imperfecta hypomaturation type IIA2
  • amelogenesis imperfecta pigmented hypomaturation type 2
  • amelogenesis imperfecta type IIA2
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the matrix metalloproteinase-20 gene (MMP20).
Super Class
amelogenesis imperfecta autosomal recessive disease
External Links
Disease Ontology
DOID:0110060
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
1645 AKR1C1 aldo-keto reductase family 1 member C1
1646 AKR1C2 aldo-keto reductase family 1 member C2
55858 TMEM165 transmembrane protein 165
64386 MMP25 matrix metallopeptidase 25

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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: August 19, 2024