Amelogenesis Imperfecta, Type Ic; Ai1c
Clinical Features
Phenotypes and symptoms related to Amelogenesis Imperfecta, Type Ic; Ai1c
- Dental malocclusion
- Hypoplasia of dental enamel
- Open bite
- Amelogenesis imperfecta
- Taurodontia
- Anterior open bite
- Yellow-brown discoloration of the teeth
- Anterior open-bite malocclusion
- 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.
Alternative names
Amelogenesis Imperfecta, Type Ic; Ai1c Is also known as amelogenesis imperfecta, hypoplastic, with or without openbite malocclusion, autosomal recessive, amelogenesis imperfecta, local hypoplastic type, autosomal recessive.
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, Type Ic; Ai1c Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Amelogenesis Imperfecta via ENAM Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
ENAM
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 1C.
By Centogene AG - the Rare Disease Company (Germany).
ENAM
Specificity
100 %
Genes
100 % |
Amelogenesis imperfecta, type 1B.
By Centogene AG - the Rare Disease Company (Germany).
ENAM
Specificity
100 %
Genes
100 % |
You can get up to 13 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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