MMP20 gene related symptoms and diseases
All the information presented here about the MMP20 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,ORPHANET,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to MMP20 gene
Symptoms // Phenotype | % Cases |
---|---|
Carious teeth | Uncommon - Between 30% and 50% cases |
Open bite | Uncommon - Between 30% and 50% cases |
Amelogenesis imperfecta | Uncommon - Between 30% and 50% cases |
Overbite | Uncommon - Between 30% and 50% cases |
Anterior open bite | Uncommon - Between 30% and 50% cases |
Rare diseases associated to MMP20 gene
Here you will find a list of rare diseases related to the MMP20. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2
Alternate names
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2 Is also known as amelogenesis imperfecta, pigmented hypomaturation type, 2
Description
Autosomal recessive amelogenesis imperfecta pigmented hypomaturation type is characterized by enamel of normal thickness that is hypomineralized and has a mottled appearance. The slightly soft enamel detaches easily from the dentin, and radiographs show a lack of contrast between enamel and dentin (Witkop, 1989).
Most common symptoms of AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2
- Carious teeth
- Open bite
- Amelogenesis imperfecta
- Overbite
- Anterior open bite
More info about AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2
HYPOMATURATION AMELOGENESIS IMPERFECTA
Alternate names
HYPOMATURATION AMELOGENESIS IMPERFECTA Is also known as amelogenesis imperfecta type 2
More info about HYPOMATURATION AMELOGENESIS IMPERFECTA
SOURCES: ORPHANET
Search interest in MMP20
Potential gene panels for MMP20 gene
Amelogenesis Imperfecta via MMP20 Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the MMP20 gene.
More info about this panelAmelogenesis Imperfecta Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Amelogenesis Imperfecta Sequencing Panel with CNV Detection that also includes the following genes: CNNM4 SLC24A4 SMOC2 FAM20A FAM83H ODAPH WDR72 DLX3 ROGDI ENAM
More info about this panelAmelogenesis imperfecta and related disorders Deletion/ Duplication panel Panel
By Connective Tissue Gene Tests Amelogenesis imperfecta and related disorders Deletion/ Duplication panel that also includes the following genes: SLC24A4 SMOC2 FAM20A FAM83H ODAPH WDR72 DLX3 DSPP ENAM GPR68
More info about this panelAmelogenesis imperfecta and related disorders Comprehensive panel Panel
By Connective Tissue Gene Tests Amelogenesis imperfecta and related disorders Comprehensive panel that also includes the following genes: SLC24A4 SMOC2 FAM20A FAM83H ODAPH WDR72 DLX3 DSPP ENAM GPR68
More info about this panelAmelogenesis imperfecta and related disorders NGS panel Panel
By Connective Tissue Gene Tests Amelogenesis imperfecta and related disorders NGS panel that also includes the following genes: SLC24A4 SMOC2 FAM20A FAM83H ODAPH WDR72 DLX3 DSPP ENAM GPR68
More info about this panelAmelogenesis imperfecta type 2A2 Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the MMP20 gene.
More info about this panelqGenEx Craniofacial Anomalies Panel
By Quantitative Genomic Medicine Laboratories, SL qGenEx Craniofacial Anomalies that also includes the following genes: RUNX2 SALL1 TSHZ1 BMP4 SEMA3E SF3B4 SH3BP2 SHH SIX1 SIX3
More info about this panelAmelogenesis Imperfecta NGS Panel Panel
By Fulgent Genetics Fulgent Genetics Amelogenesis Imperfecta NGS Panel that also includes the following genes: BMP1 SERPINH1 IFITM5 SP7 FKBP10 P3H1 COL1A2 FAM20A CRTAP FAM83H
More info about this panelMMP20 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the MMP20 gene.
More info about this panelAmelogenesis Imperfecta and Dentinogenesis Imperfecta Panel Panel
By Blueprint Genetics Amelogenesis Imperfecta and Dentinogenesis Imperfecta Panel that also includes the following genes: SLC24A4 FAM20A FAM83H ODAPH WDR72 DLX3 DSPP ENAM GPR68 AMELX
More info about this panelAmelogenesis Imperfecta , Panel Massive Sequencing (NGS) 9 Genes Panel
By Reference Laboratory Genetics Amelogenesis Imperfecta , Panel Massive Sequencing (NGS) 9 Genes that also includes the following genes: FAM20A FAM83H WDR72 DLX3 ENAM AMELX KLK4 LAMB3 MMP20
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