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.
Thyrotoxic periodic paralysis
Very frequent (80-99%)
Arachnoid cyst
Occasional (5-29%)
Nelson syndrome
Frequent (30-79%)
Roussy-Lévy syndrome
Frequent (30-79%)
Kugelberg-Welander disease
Always present (100%)
Cholestanol storage disease
Always present (100%)
Adrenoleukodystrophy
Gerstmann-Straussler-Scheinker syndrome
Very frequent (80-99%)
Amyotrophic lateral sclerosis
Frequent (30-79%)
Tay-Sachs disease
Frequent (30-79%)
Nemaline myopathy, late onset type
Occasional (5-29%)
Early onset cerebellar ataxia with retained tendon reflexes
Occasional (5-29%)
Silver disease
Troyer syndrome
Always present (100%)
Parkes Weber syndrome
Occasional (5-29%)
Mitochondrial trifunctional protein deficiency
Frequent (30-79%)
Peripheral neuroectodermal tumour
Occasional (5-29%)
Glycogen heart disease
Frequent (30-79%)
Eosinophilic myositis
Frequent (30-79%)
Acute poliomyelitis
Frequent (30-79%)
Fragile X associated tremor ataxia syndrome
Frequent (30-79%)
HCC - hypomyelination and congenital cataract
Very frequent (80-99%)
Hereditary inclusion body myopathy
Very frequent (80-99%)
Jankovic-Rivera syndrome
Very frequent (80-99%)
Cap myopathy
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 1137412000
- UMLS CUI
- C1836296
- Fully Specified Name
- Weakness of muscle of lower limb (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.