| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Injury of muscle(s) and tendon(s) of anterior muscle group at lower leg level | Finding site | False | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Injury of muscle(s) and tendon(s) of peroneal muscle group at lower leg level | Finding site | False | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Injury of muscle and tendon at ankle and foot level | Finding site | False | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Injury of muscle and tendon of long flexor muscle of toe at ankle and foot level | Finding site | False | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Injury of muscle and tendon of long extensor muscle of toe at ankle and foot level | Finding site | False | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Structure of extraocular muscle | Is a | True | Skeletal muscle structure | Inferred relationship | Some |  | 
| Orbital myositis of left eye | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Orbital myositis of right eye | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Bilateral orbital myositis of eyes | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Rhabdomyolysis due to disease caused by severe acute respiratory syndrome coronavirus 2 (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Myopathy due to calcium deficiency (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Huntington's chorea | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Juvenile onset Huntington's disease | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 6 | 
| Late onset Huntington's disease | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 6 | 
| Akinetic-rigid form of Huntington's disease | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 6 | 
| Hypotonic-hyporesponsive episode (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital muscular dystrophy type 1D large gene mutation (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Crush syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Neostigmine test | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Ice pack test | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Crush syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Paresis of left vocal cord (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Paresis of right vocal cord (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Bilateral partial vocal cord paralysis | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Nontraumatic intramuscular haematoma | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Fibrous dysplasia of bone with intramuscular myxoma | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Neonatal neuromuscular disorder | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Hypomyopathic juvenile dermatomyositis | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Juvenile dermatomyositis overlap syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Juvenile polymyositis due to paraneoplastic syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Polymyositis overlap syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Dermatomyositis overlap syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Sporadic inclusion body myositis (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Paroxysmal rhabdomyolysis (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 5 | 
| Myofascial pain syndrome of neck | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Autosomal recessive Emery-Dreifuss muscular dystrophy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| X-linked Emery-Dreifuss muscular dystrophy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Glycogen storage disease due to muscle beta-enolase deficiency | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Mycobacterial myositis | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Adenylosuccinate synthetase-like 1-related distal myopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| POGLUT1-related limb girdle muscular dystrophy R21 | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Allan-Herndon-Dudley syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Mitochondrial myopathy, lactic acidosis, deafness syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Combined oxidative phosphorylation defect type 30 | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Congenital generalized hypercontractile muscle stiffness syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Myotonic dystrophy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| LIMS2-related limb girdle muscular dystrophy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Glycogen storage disease due to lactate dehydrogenase deficiency | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Intellectual disability, epilepsy, extrapyramidal syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Maternally inherited mitochondrial myopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Maternally inherited mitochondrial cardiomyopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Mitochondrial respiratory chain complex I structural subunit gene defect | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Mitochondrial respiratory chain complex I assembly gene defect | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with methylmalonic aciduria (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Typical nemaline myopathy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Childhood-onset nemaline myopathy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Actin accumulation myopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Amish nemaline myopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Intermediate nemaline myopathy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Severe congenital nemaline myopathy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Proximal myopathy with focal depletion of mitochondria | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Autosomal recessive central core disease | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal dominant central core disease (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital fiber-type disproportion myopathy due to ZAK mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital fiber-type disproportion myopathy due to SELENON mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal dominant congenital fibre-type disproportion myopathy due to SELENON mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal recessive congenital fiber-type disproportion myopathy due to selenoprotein N mutation (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital fibre-type disproportion myopathy due to ACTA1 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal recessive congenital fibre-type disproportion myopathy due to ACTA1 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital fiber-type disproportion myopathy due to TPM3 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Autosomal dominant congenital fiber-type disproportion myopathy due to TPM3 mutation | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Myasthenia gravis in remission | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Klippel-Feil anomaly, myopathy, facial dysmorphism syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Progressive scapulohumeroperoneal distal myopathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Autosomal dominant mitochondrial myopathy with exercise intolerance | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 4 | 
| Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Intramuscular injection of human anti-D immunoglobulin | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Polyglucosan body myopathy type 2 | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Megaconial congenital muscular dystrophy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Megaconial congenital muscular dystrophy | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Hereditary continuous muscle fiber activity | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 |