Related Conditions
Azoospermia with absent vasa in association with cystic fibrosis trait(child)
Male infertility with oligozoospermia due to single gene mutation(child)
Male infertility with teratozoospermia due to single gene mutation(child)
Male infertility with azoospermia due to single gene mutation(child)
Primary male infertility(parent)
Genetic disease(parent)
Quick Facts
- SNOMED CT
- 236792002
- UMLS CUI
- C0403804
- Fully Specified Name
- Male infertility of genetic origin (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.