GPR68 gene related symptoms and diseases
All the information presented here about the GPR68 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to GPR68 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Open bite | Uncommon - Between 30% and 50% cases |
| Amelogenesis imperfecta | Uncommon - Between 30% and 50% cases |
| Anterior open bite | Uncommon - Between 30% and 50% cases |
Rare diseases associated to GPR68 gene
Here you will find a list of rare diseases related to the GPR68. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6
Description
Autosomal recessive amelogenesis imperfecta of the 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, IIA6; AI2A6
- Open bite
- Amelogenesis imperfecta
- Anterior open bite
More info about AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6
SOURCES: OMIM
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 GPR68
Potential gene panels for GPR68 gene
Amelogenesis Imperfecta Sequencing Panel with CNV Detection Panel
United States.
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 panel United States.
Amelogenesis imperfecta and related disorders Deletion/ Duplication panel Panel
United States.
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 panel United States.
Amelogenesis imperfecta and related disorders Comprehensive panel Panel
United States.
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 panel United States.
Amelogenesis imperfecta and related disorders NGS panel Panel
United States.
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 panel United States.
GPR68 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the GPR68 gene.
More info about this panel United States.
Amelogenesis Imperfecta and Dentinogenesis Imperfecta Panel Panel
Finland.
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 panel Finland.
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