Phenotypes associated with the disease spermatogenic failure 31 (OMIM:618112):
- Male infertility (HP:0003251). Evidence: PCS. Frequency: 5/5. (PMID:30032984)
- Male infertility (HP:0003251). Evidence: PCS. Frequency: 2/2. (PMID:30298696)
- 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:30032984)
- Acephalic spermatozoa (HP:0012869): Spermatozoa with very small cranial ends devoid of any nuclear material, that is, lacking a typical sperm head. Evidence: PCS. Frequency: 5/5. (PMID:30032984)
- Acephalic spermatozoa (HP:0012869): Spermatozoa with very small cranial ends devoid of any nuclear material, that is, lacking a typical sperm head. Evidence: PCS. Frequency: 2/2. (PMID:30298696)