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.
Hypercortisolism due to nonpituitary tumor
Frequent (30-79%)
Childhood type dermatomyositis
Very frequent (80-99%)
Neurogenic thoracic outlet syndrome
Frequent (30-79%)
Arachnoiditis
Very frequent (80-99%)
Distichiasis-lymphedema syndrome
Frequent (30-79%)
Myotonia levior
Excluded (<1%)
Hyperphosphatasemia with bone disease
Friedreich's ataxia
Frequent (30-79%)
Glycogen storage disease, type IV
Coffin-Lowry syndrome
Occasional (5-29%)
Atrophia bulborum hereditaria
Occasional (5-29%)
Pseudohypoaldosteronism, type 2
Occasional (5-29%)
Cyclical vomiting syndrome
Lassa fever
Frequent (30-79%)
Triglyceride storage disease with ichthyosis
Congenital myotonia, autosomal recessive form
Always present (100%)
Renal carnitine transport defect
Very frequent (80-99%)
Glutaric aciduria, type 2
Lyme disease
Occasional (5-29%)
Sandhoff disease
Frequent (30-79%)
Metachromatic leukodystrophy, adult type
Frequent (30-79%)
Severe adrenal insufficiency
Very frequent (80-99%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Occasional (5-29%)
Kearns-Sayre syndrome
Occasional (5-29%)
African trypanosomiasis
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 26544005
- UMLS CUI
- C0151786
- Fully Specified Name
- Muscle weakness (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.