heterotaxy, visceral, 13, autosomal
MONDO:0976134Mondo
Findings
No curated finding names heterotaxy, visceral, 13, autosomal 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
27 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.
- AspleniaHPOHP:0001746
- 1 of 1 reported patient
- Bronchial isomerismHPOHP:0031564
- 1 of 1 reported patient
- CardiomegalyHPOHP:0001640
- 1 of 1 reported patient
- CardiomyopathyHPOHP:0001638
- 1 of 1 reported patient
- Coarse facial featuresHPOHP:0000280
- 1 of 1 reported patient
- Complete atrioventricular canal defectHPOHP:0001674
- 2 of 2 reported patients
- Congestive heart failureHPOHP:0001635
- 1 of 1 reported patient
- Delayed fine motor developmentHPOHP:0010862
- 1 of 1 reported patient
- Delayed speech and language developmentHPOHP:0000750
- 1 of 1 reported patient
- DextrocardiaHPOHP:0001651
- 1 of 1 reported patient
- DyskinesiaHPOHP:0100660
- 1 of 1 reported patient
- EpicanthusHPOHP:0000286
- 1 of 1 reported patient
Show the remaining 15
- Global developmental delayHPOHP:0001263
- 1 of 1 reported patient
- HypertelorismHPOHP:0000316
- 1 of 1 reported patient
- Infracardiac total anomalous pulmonary venous connectionHPOHP:0011721
- 1 of 1 reported patient
- Intestinal malrotationHPOHP:0002566
- 1 of 1 reported patient
- IsomerismHPOHP:0031853
- 1 of 1 reported patient
- Nasogastric tube feedingHPOHP:0040288
- 1 of 1 reported patient
Where it sits
- A kind of