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.
Meconium aspiration syndrome
Frequent (30-79%)
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Occasional (5-29%)
Idiopathic neonatal atrial flutter
Occasional (5-29%)
FRAXE intellectual disability syndrome
Occasional (5-29%)
Congenital infection caused by enterovirus
Occasional (5-29%)
Congenital lactic acidosis Saguenay-Lac-Saint-Jean type
Frequent (30-79%)
X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome
Occasional (5-29%)
Infantile osteopetrosis with neuroaxonal dysplasia syndrome
Occasional (5-29%)
Pyridoxine-dependent epilepsy
Tatton Brown Rahman overgrowth syndrome
Always present (100%)
Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome
Occasional (5-29%)
Autoinflammatory disease due to interleukin-1 receptor antagonist deficiency
Frequent (30-79%)
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
Occasional (5-29%)
Ubiquitin specific peptidase 18 deficiency
Always present (100%)
Quick Facts
- SNOMED CT
- 130955003
- UMLS CUI
- C0015930
- Fully Specified Name
- Fetal distress (finding)
- Associated Conditions
- 14
- 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.