# tetralogy of Fallot

> congenital heart defect, whose symptoms include episodes of bluish skin color, whose embryology includes anteriosuperior displacement of the infundibular (aorticopulmonary) septum

**Wikidata**: [Q1126831](https://www.wikidata.org/wiki/Q1126831)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Tetralogy_of_Fallot)  
**Source**: https://4ort.xyz/entity/tetralogy-of-fallot


## References

1. [Source](http://www.nanbyou.or.jp/entry/4741)
2. [Source](https://ddrare.nibiohn.go.jp/)
3. Monarch Disease Ontology release 2018-06-29
4. [Nuovo soggettario](https://thes.bncf.firenze.sbn.it/termine.php?id=27155)
5. Disease Ontology
6. Nuovo soggettario
7. [Source](http://www.patient.co.uk/patientplus/f.htm)
8. NDF-RT
9. [Phenocarta](https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6419&ncbiId=8829)
10. [Phenocarta](https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_6419&ncbiId=2262)
11. UniProt
12. Familial Tetralogy of Fallot caused by mutation in the jagged1 gene
13. GATA4 sequence variants in patients with congenital heart disease
14. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
15. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
16. Identification of GATA6 sequence variants in patients with congenital heart defects.
17. Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.
18. YSO-Wikidata mapping project
19. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)
20. Human Phenotype Ontology release 2018-03-08
21. Quora
22. National Library of Israel