spermatogenic failure 47
MONDO:0030844Mondo
Findings
No curated finding names spermatogenic failure 47 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
5 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 flagellaHPOHP:0032558
- 2 of 2 reported patients
- Immotile spermHPOHP:0012208
- 2 of 2 reported patients
- Male infertilityHPOHP:0003251
- 2 of 2 reported patients
- OligozoospermiaHPOHP:0000798
- 2 of 2 reported patients
- Short sperm flagellaHPOHP:0032559
- 2 of 2 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- DZIP1HGNC:20908
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
Where it sits
- A kind of
Other names
1 name
Resolves to: spermatogenic failure 47
- Also called
- SPGF47