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.
Childhood type dermatomyositis
Frequent (30-79%)
Neurogenic thoracic outlet syndrome
Occasional (5-29%)
Primary intestinal lymphangiectasia
Occasional (5-29%)
Friedreich's ataxia
Frequent (30-79%)
Neuroleptic malignant syndrome
Frequent (30-79%)
Fabry's disease
Thyrotoxic periodic paralysis
Frequent (30-79%)
Post poliomyelitis syndrome
Occasional (5-29%)
Stress polycythemia
Frequent (30-79%)
Pseudohypoparathyroidism type II
Occasional (5-29%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Kugelberg-Welander disease
Frequent (30-79%)
Hereditary xanthinuria
Occasional (5-29%)
Pseudohypoparathyroidism type I B
Occasional (5-29%)
Congenital myotonia, autosomal dominant form
Occasional (5-29%)
Pseudohypoparathyroidism type I A
Occasional (5-29%)
Cholera
Frequent (30-79%)
Reye's syndrome
Occasional (5-29%)
Autoimmune hypoparathyroidism
Occasional (5-29%)
Neu-Laxova syndrome
Frequent (30-79%)
Isaacs syndrome
Frequent (30-79%)
Familial hypokalemic alkalosis, Gullner type
Familial hypokalemic periodic paralysis
Occasional (5-29%)
Amyotrophic lateral sclerosis
Frequent (30-79%)
Azorean disease
Quick Facts
- SNOMED CT
- 45352006
- UMLS CUI
- C0037763
- Fully Specified Name
- Spasm (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.