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.
Listeriosis
Very rare (1-4%)
Tuberous sclerosis syndrome
Occasional (5-29%)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Desquamative interstitial pneumonia
Biotinidase deficiency
Occasional (5-29%)
Congenital stenosis of trachea
Frequent (30-79%)
Glycogen storage disease, type IV
Occasional (5-29%)
Woolsorters' disease
Frequent (30-79%)
Acute neuronopathic Gaucher's disease
Frequent (30-79%)
Congenital diaphragmatic hernia
Frequent (30-79%)
Toxic shock syndrome
Frequent (30-79%)
Schinzel-Giedion syndrome
Occasional (5-29%)
Tularemia
Occasional (5-29%)
Renal carnitine transport defect
Occasional (5-29%)
Glutaric aciduria, type 2
Poisoning by colchicine
Very frequent (80-99%)
Congenital atresia of esophagus
Occasional (5-29%)
Cocaine intoxication
Very rare (1-4%)
Fructose-biphosphatase deficiency
Occasional (5-29%)
Nocardiosis
Occasional (5-29%)
Ventricular septal defect
Frequent (30-79%)
Laryngomalacia
Pachyonychia congenita syndrome
Very rare (1-4%)
Scimitar syndrome
Occasional (5-29%)
Cryptococcosis
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 271825005
- UMLS CUI
- C0476273
- Fully Specified Name
- Respiratory distress (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.