spermatogenic failure 51
MONDO:0030926Mondo
Findings
No curated finding names spermatogenic failure 51 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
9 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Absent sperm axoneme central pair complexHPOHP:0033525
- 6 of 6 reported patients
- Absent sperm flagellaHPOHP:0032558
- 6 of 6 reported patients
- Coiled sperm flagellaHPOHP:0032560
- 6 of 6 reported patients
- Irregularly shaped sperm tailHPOHP:0033393
- 6 of 6 reported patients
- MacrozoospermiaHPOHP:0025437
- 6 of 6 reported patients
- Microcephalic sperm headHPOHP:0032561
- 6 of 6 reported patients
- Reduced sperm motilityHPOHP:0012207
- 6 of 6 reported patients
- Short sperm flagellaHPOHP:0032559
- 6 of 6 reported patients
- OligozoospermiaHPOHP:0000798
- 3 of 6 reported patients
Where it sits
- A kind of
Other names
1 name
Resolves to: spermatogenic failure 51
- Also called
- SPGF51