Phenotypes associated with the disease spermatogenic failure, Y-linked, 2 (OMIM:415000):
- Y-linked inheritance (HP:0001450): A mode of inheritance that is observed for traits related to a gene encoded on the Y chromosome. Evidence: IEA. (OMIM:415000)
- Male infertility (HP:0003251). Evidence: TAS. (OMIM:415000)
- Young adult onset (HP:0011462): Onset of disease at the age of between 16 and 40 years. Evidence: TAS. (OMIM:415000)
- Azoospermia (HP:0000027): Absence of any measurable level of sperm,whereby spermatozoa cannot be observed even after centrifugation of the semen pellet. Evidence: IEA. (OMIM:415000)