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.
Kugelberg-Welander disease
Hemiplegic migraine
Frequent (30-79%)
Werdnig-Hoffmann disease
Amyotrophic lateral sclerosis
Occasional (5-29%)
Déjérine-Sottas disease
Always present (100%)
SMA2
Autosomal dominant sensory neuropathy
Always present (100%)
Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency
Always present (100%)
Glycogen heart disease
Frequent (30-79%)
Hereditary sensory and autonomic neuropathy type I
Always present (100%)
Jankovic-Rivera syndrome
Frequent (30-79%)
Sudden infant death with dysgenesis of testes syndrome
Spinocerebellar ataxia type 36
Frequent (30-79%)
Charcot-Marie-Tooth disease type 4C
Congenital pontocerebellar hypoplasia type 7
Occasional (5-29%)
Congenital pontocerebellar hypoplasia type 1
Occasional (5-29%)
X-linked distal arthrogryposis multiplex congenita
Occasional (5-29%)
Severe X-linked mitochondrial encephalomyopathy
Frequent (30-79%)
Spastic paraplegia with Paget disease of bone syndrome
Frequent (30-79%)
Intellectual disability, hypotonia, facial dysmorphism syndrome
Occasional (5-29%)
Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability
Occasional (5-29%)
Combined oxidative phosphorylation defect type 11
Frequent (30-79%)
Lower motor neuron syndrome with late-adult onset
Occasional (5-29%)
Hereditary sensory autonomic neuropathy type IA
Always present (100%)
Proximal spinal muscular atrophy
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 249878001
- UMLS CUI
- C0239548
- Fully Specified Name
- Fasciculation of tongue (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.