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.
Locked in syndrome
Very frequent (80-99%)
Adult onset basal ganglia disease
Fatty acid hydroxylase associated neurodegeneration
Frequent (30-79%)
Infantile-onset ascending hereditary spastic paralysis
Very frequent (80-99%)
Juvenile amyotrophic lateral sclerosis
Occasional (5-29%)
X-linked distal arthrogryposis multiplex congenita
Frequent (30-79%)
Kufor Rakeb syndrome
Frequent (30-79%)
Atypical juvenile parkinsonism
Occasional (5-29%)
Parkinsonism caused by cyanide
Frequent (30-79%)
Dystonia aphonia syndrome
Frequent (30-79%)
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
Occasional (5-29%)
Cataracts, motor neuropathy, short stature, skeletal anomalies syndrome
Occasional (5-29%)
Juvenile amyotrophic lateral sclerosis type 2
Frequent (30-79%)
Dystonia 28
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 48257004
- UMLS CUI
- C0234517
- Fully Specified Name
- Anarthria (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.