Spermatogenic Failure X Linked 2 C1839841
An inherited form of male infertility caused by mutations on the X chromosome that disrupt normal sperm development. This X-linked condition affects only males and often requires assisted reproduction.
Key facts at a glance
- ICD-10
- Q55.9
- ICD-11
- LA00.0
- Body system
- reproductive
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy