heterotaxy, visceral, 9, autosomal, with male infertility
MONDO:0030070Mondo
Findings
No curated finding names heterotaxy, visceral, 9, autosomal, with male infertility yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Antenatal onset
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.
- Male infertilityHPOHP:0003251
- 3 of 3 reported patients · Male
- DextrocardiaHPOHP:0001651
- 1 of 4 reported patients · Antenatal onset
- 5 of 7 reported patients
- Situs inversus totalisHPOHP:0001696
- 7 of 11 reported patients
- Recurrent otitis mediaHPOHP:0000403
- 1 of 6 reported patients
- AspleniaHPOHP:0001746
- 1 of 7 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.
- MNS1HGNC:29636
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
1 name
Resolves to: heterotaxy, visceral, 9, autosomal, with male infertility
- Also called
- HTX9