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.
Ehlers-Danlos syndrome, type 3
Frequent (30-79%)
Sarcotubular myopathy
Glycogen storage disease, type V
Occasional (5-29%)
Muscle phosphoglycerate mutase deficiency
Reye's syndrome
Frequent (30-79%)
Glycogen storage disease, type VII
Frequent (30-79%)
Deficiency of adenylic acid deaminase
Very frequent (80-99%)
MCAD deficiency
Frequent (30-79%)
Hereditary liability to pressure palsies
Occasional (5-29%)
Very long chain acyl-CoA dehydrogenase deficiency
CPTII - Carnitine palmitoyltransferase deficiency type II
Frequent (30-79%)
Hutterite type of muscular dystrophy
Myopathy with tubular aggregates
Distal myopathy with vocal cord weakness
Frequent (30-79%)
Rippling muscle disease
Familial partial lipodystrophy type 2
Always present (100%)
Atypical Werner syndrome
Occasional (5-29%)
Autosomal dominant centronuclear myopathy
Occasional (5-29%)
Genetic recurrent myoglobinuria
Frequent (30-79%)
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Frequent (30-79%)
Autosomal recessive limb girdle muscular dystrophy type 2L
Frequent (30-79%)
Distal myopathy with posterior leg and anterior hand involvement
Very frequent (80-99%)
King Denborough syndrome
Occasional (5-29%)
Distal myopathy with anterior tibial onset
Frequent (30-79%)
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Quick Facts
- SNOMED CT
- 1141861001
- UMLS CUI
- C1850830
- Fully Specified Name
- Exercise induced myalgia (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.