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.
Schwartz-Jampel syndrome
Frequent (30-79%)
Sarcotubular myopathy
Inclusion body myositis
Very frequent (80-99%)
Hutterite type of muscular dystrophy
Tibial muscular dystrophy
Occasional (5-29%)
MPRM - myopathy, proximal, with early respiratory muscle involvement
Charcot-Marie-Tooth disease type 4A
Occasional (5-29%)
Bethlem myopathy
Frequent (30-79%)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
Frequent (30-79%)
Pure mitochondrial myopathy
Occasional (5-29%)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2
Occasional (5-29%)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
Occasional (5-29%)
Miyoshi muscular dystrophy type 3
Frequent (30-79%)
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Always present (100%)
Autosomal dominant progressive external ophthalmoplegia
Frequent (30-79%)
Proximal spinal muscular atrophy
Frequent (30-79%)
ADSSL1-related distal myopathy
Frequent (30-79%)
Autosomal dominant Charcot-Marie-Tooth disease type 2Y
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 300948004
- UMLS CUI
- C0577655
- Fully Specified Name
- Quadriceps weakness (finding)
- Associated Conditions
- 18
- 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.