DDX3Y gene related symptoms and diseases
All the information presented here about the DDX3Y gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,ORPHANET,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to DDX3Y gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Cryptorchidism | Very Common - Between 80% and 100% cases |
| Decreased testicular size | Very Common - Between 80% and 100% cases |
| Male infertility | Very Common - Between 80% and 100% cases |
| Oligospermia | Very Common - Between 80% and 100% cases |
| Abnormal spermatogenesis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with DDX3Y gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Non-obstructive azoospermia
Rare diseases associated to DDX3Y gene
Here you will find a list of rare diseases related to the DDX3Y. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
PARTIAL CHROMOSOME Y DELETION
Alternate names
PARTIAL CHROMOSOME Y DELETION Is also known as male sterility due to chromosome y deletion
Description
Male sterility due to chromosome Y deletion is characterized by a severe deficiency of spermatogenesis. Chromosome Y deletions are a frequent genetic cause of male infertility.
Most common symptoms of PARTIAL CHROMOSOME Y DELETION
- Cryptorchidism
- Decreased testicular size
- Male infertility
- Oligospermia
- Abnormal spermatogenesis
More info about PARTIAL CHROMOSOME Y DELETION
SOURCES: ORPHANET
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