ACP4 gene related symptoms and diseases
All the information presented here about the ACP4 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to ACP4 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Carious teeth | Uncommon - Between 30% and 50% cases |
| Amelogenesis imperfecta | Uncommon - Between 30% and 50% cases |
| Overbite | Uncommon - Between 30% and 50% cases |
Rare diseases associated to ACP4 gene
Here you will find a list of rare diseases related to the ACP4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J
Description
Amelogenesis imperfecta is an inherited defect of dental enamel formation that shows both clinical and genetic heterogeneity. In the hypoplastic type of AI, the enamel is of normal hardness but does not develop to normal thickness. The thinness of the enamel makes the teeth appear small. Radiographically, enamel contrasts normally from dentin. The surface of the enamel can vary, showing smooth, rough, pitted, or local forms (Witkop, 1988).
Most common symptoms of AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J
- Carious teeth
- Amelogenesis imperfecta
- Overbite
More info about AMELOGENESIS IMPERFECTA, TYPE IJ; AI1J
SOURCES: OMIM
HYPOPLASTIC AMELOGENESIS IMPERFECTA
Alternate names
HYPOPLASTIC AMELOGENESIS IMPERFECTA Is also known as amelogenesis imperfecta type 1
More info about HYPOPLASTIC AMELOGENESIS IMPERFECTA
SOURCES: ORPHANET
Search interest in ACP4
Potential gene panels for ACP4 gene
ACPT Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the ACP4 gene.
More info about this panel United States.
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