amelogenesis imperfecta hypomaturation type 2A4

Summary
Synonym
  • AI2A4
  • amelogenesis imperfecta hypomaturation type IIA4
  • amelogenesis imperfecta type IIA4
Definition
An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21.
Super Class
amelogenesis imperfecta autosomal recessive disease
External Links
Disease Ontology
DOID:0110062
Mondo Disease Ontology
OMIM
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