tetralogy of Fallot
MeSH: D013771ORPHA: 3303
Overview
congenital heart defect, whose symptoms include episodes of bluish skin color, whose embryology includes anteriosuperior displacement of the infundibular (aorticopulmonary) septum
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with tetralogy of Fallot, sourced from HPO and Orphanet clinical annotations.
CryptorchidismThin vermilion borderDolichocephalyBroad foreheadProptosisBrachydactylyIntrauterine growth retardationTetralogy of FallotClinodactyly of the 5th fingerPreauricular pitAbnormal nasal morphologyUnderdeveloped supraorbital ridges
Classification & Codes
MeSH Code
D013771Orphanet Code
ORPHA:3303tetralogy of Fallot
| MeSH | D013771 |
| Orphanet | ORPHA:3303 |
| Treatments | 0 drug(s) |
| Symptoms on record | 12 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO