Amelogenesis Imperfecta, Hypomaturation Type, Iia4; Ai2a4
Genes related to Amelogenesis Imperfecta, Hypomaturation Type, Iia4; Ai2a4
- ODAPH
Clinical Features
Phenotypes and symptoms related to Amelogenesis Imperfecta, Hypomaturation Type, Iia4; Ai2a4
- Hypoplasia of dental enamel
- Amelogenesis imperfecta
- Hypomineralization of enamel
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Amelogenesis Imperfecta, Hypomaturation Type, Iia4; Ai2a4 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Amelogenesis Imperfecta via ODAPH (C4orf26) Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ODAPH
Specificity
100 %
Genes
100 % |
Amelogenesis Imperfecta Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
CNNM4, SLC24A4, SMOC2, FAM20A, FAM83H, ODAPH, WDR72, DLX3, ROGDI, ENAM, GPR68, AMELX, ITGB6, KLK4, LAMA3, LAMB3, LTBP3, MMP20
Specificity
6 %
Genes
100 % |
Amelogenesis imperfecta and related disorders Deletion/ Duplication panel.
By Connective Tissue Gene Tests (United States).
SLC24A4, SMOC2, FAM20A, FAM83H, ODAPH, WDR72, DLX3, DSPP, ENAM, GPR68, AMELX, ITGB6, KLK4, LAMA3, LAMB3, MMP20
Specificity
7 %
Genes
100 % |
Amelogenesis imperfecta and related disorders Comprehensive panel.
By Connective Tissue Gene Tests (United States).
SLC24A4, SMOC2, FAM20A, FAM83H, ODAPH, WDR72, DLX3, DSPP, ENAM, GPR68, AMELX, ITGB6, KLK4, LAMA3, LAMB3, MMP20
Specificity
7 %
Genes
100 % |
Amelogenesis imperfecta and related disorders NGS panel.
By Connective Tissue Gene Tests (United States).
SLC24A4, SMOC2, FAM20A, FAM83H, ODAPH, WDR72, DLX3, DSPP, ENAM, GPR68, AMELX, ITGB6, KLK4, LAMA3, LAMB3, MMP20
Specificity
7 %
Genes
100 % |
Amelogenesis imperfecta panel.
By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).
FAM20A, FAM83H, ODAPH, WDR72, DLX3, ENAM, AMELX, KLK4
Specificity
13 %
Genes
100 % |
Amelogenesis imperfecta type 2A4.
By Centogene AG - the Rare Disease Company (Germany).
ODAPH
Specificity
100 %
Genes
100 % |
qGenEx Craniofacial Anomalies.
By Quantitative Genomic Medicine Laboratories, SL (Spain).
RUNX2, SALL1, TSHZ1, BMP4, SEMA3E, SF3B4, SH3BP2, SHH, SIX1, SIX3, SKI, SNAI2, SMC1A, SOX10, TBX22, TCF12, TCOF1, TFAP2A, TGFBR1, TGFBR2 , (...)
View the complete list with 114 more genes
Specificity
1 %
Genes
100 % |
You can get up to 2 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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