Overview
Facial weakness 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.
X-linked centronuclear myopathy
Frequent (30-79%)
Hemiplegic migraine
Occasional (5-29%)
Cytochrome-c oxidase deficiency
Oculopharyngeal muscular dystrophy
Frequent (30-79%)
Steinert myotonic dystrophy syndrome
Frequent (30-79%)
Escobar syndrome
Frequent (30-79%)
Myasthenia gravis
Frequent (30-79%)
Deficiency of unsaturated acyl-CoA reductase
Frequent (30-79%)
Dopamine beta-hydroxylase deficiency
Frequent (30-79%)
Congenital myopathy with fibre type disproportion
Frequent (30-79%)
Dysosteosclerosis
Facioscapulohumeral muscular dystrophy
Frequent (30-79%)
Bickerstaff's brainstem encephalitis
Occasional (5-29%)
Congenital nonprogressive myopathy with Moebius and Robin sequences
Always present (100%)
Congenital bilateral perisylvian syndrome
Frequent (30-79%)
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Occasional (5-29%)
Salih congenital muscular dystrophy
Always present (100%)
Proximal myotonic myopathy
Occasional (5-29%)
Charcot-Marie-Tooth disease type 4A
Very rare (1-4%)
Charcot-Marie-Tooth disease type 4C
Occasional (5-29%)
Charcot-Marie-Tooth disease type 4B2
Occasional (5-29%)
Autosomal dominant centronuclear myopathy
Frequent (30-79%)
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
Occasional (5-29%)
Autosomal dominant optic atrophy classic form
Very rare (1-4%)
X-linked distal arthrogryposis multiplex congenita
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 95666008
- UMLS CUI
- C0427055
- Fully Specified Name
- Weakness of face muscles (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.