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.
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Pelizaeus-Merzbacher disease
Deficiency of ceruloplasmin
Gillespie syndrome
Frequent (30-79%)
ARSACS - autosomal recessive spastic ataxia of Charlevoix-Saguenay
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 10
Frequent (30-79%)
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 21
Spinocerebellar ataxia type 37
Frequent (30-79%)
Spinocerebellar ataxia type 40
Frequent (30-79%)
Autosomal recessive spinocerebellar ataxia type 7
Frequent (30-79%)
Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency
Related Symptoms
Quick Facts
- SNOMED CT
- 102935005
- UMLS CUI
- C0522198
- Fully Specified Name
- Explosive speech (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.