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

D013771

Orphanet Code

ORPHA:3303
tetralogy of Fallot
MeSHD013771
OrphanetORPHA:3303
Treatments0 drug(s)
Symptoms on record12 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO