Overview
Expressionless face is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
18p- syndrome
Frequent (30-79%)
Glycogen heart disease
Frequent (30-79%)
Adult onset basal ganglia disease
Frequent (30-79%)
Rapid onset dystonia parkinsonism
Frequent (30-79%)
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
Frequent (30-79%)
Autosomal dominant late onset Parkinson disease
Occasional (5-29%)
Cerebellar ataxia Cayman type
Always present (100%)
Brain dopamine-serotonin vesicular transport disease
Very frequent (80-99%)
Adult-onset dystonia parkinsonism
Frequent (30-79%)
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
Dopamine transporter deficiency syndrome
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 54
Occasional (5-29%)
Kufor Rakeb syndrome
Frequent (30-79%)
Atypical juvenile parkinsonism
Very frequent (80-99%)
X-linked intellectual disability Hedera type
Occasional (5-29%)
Sporadic adult-onset ataxia of unknown etiology
Occasional (5-29%)
Intellectual disability, hypotonia, facial dysmorphism syndrome
Frequent (30-79%)
HMNDYT2 - hypermanganesemia with dystonia 2
Frequent (30-79%)
X-linked parkinsonism with spasticity syndrome
Very frequent (80-99%)
Pallidopyramidal syndrome
Frequent (30-79%)
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
Frequent (30-79%)
Autosomal dominant progressive external ophthalmoplegia
Frequent (30-79%)
Sporadic infantile bilateral striatal necrosis
Occasional (5-29%)
Dopa responsive dystonia due to sepiapterin reductase deficiency
Frequent (30-79%)
Phospholipase A2 activating protein-associated neurodevelopmental disorder
Quick Facts
- SNOMED CT
- 248149005
- UMLS CUI
- C0813217
- Fully Specified Name
- Expressionless face (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.