Phenotypes associated with the disease spermatogenic failure 16 (OMIM:617187):
- Male infertility (HP:0003251). Evidence: PCS. Frequency: 8/8. (PMID:27640305)
- Young adult onset (HP:0011462): Onset of disease at the age of between 16 and 40 years. Evidence: PCS. Frequency: 8/8. (PMID:27640305)
- Autosomal recessive inheritance (HP:0000007): A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). Evidence: PCS. (PMID:27640305)
- Reduced sperm motility (HP:0012207): An abnormal reduction in the mobility of ejaculated sperm. Evidence: TAS. Frequency: 8/8. (OMIM:617187)
- Acephalic spermatozoa (HP:0012869): Spermatozoa with very small cranial ends devoid of any nuclear material, that is, lacking a typical sperm head. Evidence: TAS. Frequency: 8/8. (OMIM:617187)