Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Robin sequence
Occasional (5-29%)
Double outlet left ventricle
Frequent (30-79%)
Double outlet right ventricle
Very frequent (80-99%)
Desquamative interstitial pneumonia
Congenital stenosis of trachea
Occasional (5-29%)
Osler hemorrhagic telangiectasia syndrome
Asbestosis
Occasional (5-29%)
Congenital atresia of esophagus
Occasional (5-29%)
Dihydrolipoamide dehydrogenase deficiency
Always present (100%)
Ventricular septal defect
Occasional (5-29%)
Hereditary factor I deficiency disease
Very frequent (80-99%)
Congenital pulmonary lymphangiectasis
Very frequent (80-99%)
Common ventricle
Occasional (5-29%)
Congenital heart block
Occasional (5-29%)
Congenital emphysema
Frequent (30-79%)
Goodpasture's syndrome
Common truncus arteriosus
Very frequent (80-99%)
Congenital atresia of tricuspid valve
Very frequent (80-99%)
Congenital lobar emphysema
Frequent (30-79%)
Congenital absence of adrenal gland
Corrected transposition of great vessels
Occasional (5-29%)
Agenesis of pulmonary artery
Occasional (5-29%)
Pulmonary alveolar microlithiasis
Occasional (5-29%)
Cardiogenic shock
Frequent (30-79%)
Congenital tracheomalacia
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 3415004
- UMLS CUI
- C0010520
- Fully Specified Name
- Cyanosis (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.