DAZ3 gene related symptoms and diseases

All the information presented here about the DAZ3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,ORPHANET,OMIM, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to DAZ3 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 DAZ3 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Non-obstructive azoospermia
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Rare diseases associated to DAZ3 gene

Here you will find a list of rare diseases related to the DAZ3. 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




If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like BCAT2 CDCA7

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more