heterotaxy, visceral, 11, autosomal, with male infertility
MONDO:0030475Mondo
Findings
No curated finding names heterotaxy, visceral, 11, 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
- Congenital onset
HPO, annotations 2026-09-02
Features
11 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.
- AsthenopiaHPOHP:0031590
- 1 of 1 reported patient · Male
- Chronic sinusitisHPOHP:0011109
- 2 of 2 reported patients
- Reduced progressive sperm motilityHPOHP:0034011
- 1 of 1 reported patient
- Situs inversus totalisHPOHP:0001696
- 3 of 3 reported patients
- Chronic otitis mediaHPOHP:0000389
- 2 of 3 reported patients
- Duodenal atresiaHPOHP:0002247
- 1 of 3 reported patients
- Intestinal malrotationHPOHP:0002566
- 1 of 3 reported patients
- Partial atrioventricular canal defectHPOHP:0011577
- 1 of 3 reported patients
- PolyspleniaHPOHP:0001748
- 1 of 3 reported patients
- Primum atrial septal defectHPOHP:0010445
- 1 of 3 reported patients
- Decreased nasal nitric oxideHPOHP:0033036
- 0 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.
- CFAP45HGNC:17229
- Moderate · Ambry Genetics · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
1 name
Resolves to: heterotaxy, visceral, 11, autosomal, with male infertility
- Also called
- HTX11