SLC26A8 gene related symptoms and diseases
All the information presented here about the SLC26A8 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 SLC26A8 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Infertility | Uncommon - Between 30% and 50% cases |
| Oligospermia | Uncommon - Between 30% and 50% cases |
| Abnormality of the head | Uncommon - Between 30% and 50% cases |
Rare diseases associated to SLC26A8 gene
Here you will find a list of rare diseases related to the SLC26A8. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SPERMATOGENIC FAILURE 3; SPGF3
Description
In spermatogenic failure-3, primary infertility is associated with nonobstructive asthenozoospermia (Dirami et al., 2013).For a discussion of phenotypic and genetic heterogeneity of spermatogenic failure, see SPGF1 (OMIM ).
Most common symptoms of SPERMATOGENIC FAILURE 3; SPGF3
- Infertility
- Oligospermia
- Abnormality of the head
More info about SPERMATOGENIC FAILURE 3; SPGF3
NON-SYNDROMIC MALE INFERTILITY DUE TO SPERM MOTILITY DISORDER
Alternate names
NON-SYNDROMIC MALE INFERTILITY DUE TO SPERM MOTILITY DISORDER Is also known as non-syndromic male infertility due asthenozoospermia
Description
Non-syndromic male infertility due to sperm motility disorder is a rare, genetic, non-syndromic male infertility disorder characterized by infertility due to sperm with defects in their cilia/flagella structure, leading to absent motility or reduced forward motility in fresh ejaculate. Reduced semen volume, oligospermia and an increased number of abnormally structured spermatozoa is often present.
More info about NON-SYNDROMIC MALE INFERTILITY DUE TO SPERM MOTILITY DISORDER
SOURCES: ORPHANET
Search interest in SLC26A8
Potential gene panels for SLC26A8 gene
Male Infertility Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Male Infertility Sequencing Panel with CNV Detection that also includes the following genes: SEMA3A SEMA3E FOXL2 BRDT SOX10 SOX2 SOX3 SOX9 SRA1 SRD5A2
More info about this panel United States.
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP15 BMP4 SEMA3A SEMA3E BMP7 FOXL2 BRDT SOS1
More info about this panel United States.
SLC26A8 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SLC26A8 gene.
More info about this panel United States.
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