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Tetralogy of Fallot

disorder
SNOMED 86299006CUI C0039685

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Treatments & Interventions

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal nasal morphology
Very frequent (80-99%)HP:0005105
Bilateral fifth digit clinodactyly
Very frequent (80-99%)HP:0004209
Brachydactyly
Very frequent (80-99%)HP:0001156
Increased width of the forehead
Very frequent (80-99%)HP:0000337
Small for gestational age infant
Very frequent (80-99%)HP:0001511
Cryptorchidism
Frequent (30-79%)HP:0000028
Decreased volume of lip vermillion
Frequent (30-79%)HP:0000233
Dolichocephaly
Frequent (30-79%)HP:0000268
Preauricular fistulas
Frequent (30-79%)HP:0004467
Prominent globes
Frequent (30-79%)HP:0000520
Tetrology of fallot
Frequent (30-79%)HP:0001636
Underdeveloped brows
Frequent (30-79%)HP:0009891

Quick Facts

SNOMED CT
86299006
UMLS CUI
C0039685
Fully Specified Name
Tetralogy of Fallot (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
12
Known Treatments
1
Clinical Trials
1
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.