CLDN10 gene related symptoms and diseases
All the information presented here about the CLDN10 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CLDN10 gene
Symptoms // Phenotype | % Cases |
---|---|
Pain | Very Common - Between 80% and 100% cases |
Polyuria | Very Common - Between 80% and 100% cases |
Hypermagnesemia | Very Common - Between 80% and 100% cases |
Secondary hyperparathyroidism | Very Common - Between 80% and 100% cases |
Hypocalciuria | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with CLDN10 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Alacrima
- Heat intolerance
- Xerostomia
- Hyperparathyroidism
- Anhidrosis
- Hypokalemia
- Renal insufficiency
- Cachexia
And 8 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CLDN10 gene
Here you will find a list of rare diseases related to the CLDN10. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
HELIX SYNDROME; HELIX
Alternate names
HELIX SYNDROME; HELIX Is also known as hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, and xerostomia
Most common symptoms of HELIX SYNDROME; HELIX
- Pain
- Renal insufficiency
- Dry skin
- Ichthyosis
- Postural instability
More info about HELIX SYNDROME; HELIX
SOURCES: OMIM
Search interest in CLDN10
Potential gene panels for CLDN10 gene
Hereditary kidney disorders - different panels Panel
By Institute of Human Genetics Uniklinik RWTH Aachen Hereditary kidney disorders - different panels that also includes the following genes: BCS1L ROBO2 CNNM2 CFB SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8
More info about this panelCLDN10 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CLDN10 gene.
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