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.
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Occasional (5-29%)
Sotos' syndrome
Always present (100%)
Koolen De Vries syndrome
Occasional (5-29%)
Wilson Turner syndrome
Frequent (30-79%)
Familial hypertryptophanemia
Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome
Occasional (5-29%)
Autosomal recessive spinocerebellar ataxia type 21
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 39423001
- UMLS CUI
- C0038506
- Fully Specified Name
- Stuttering (finding)
- Associated Conditions
- 7
- 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.