| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Hereditary continuous muscle fiber activity | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| TK2-related mitochondrial deoxyribonucleic acid depletion syndrome myopathic form (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Myopathy caused by local anesthetic | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Adult-onset overlap myositis | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Limb girdle muscular dystrophy due to POMK deficiency | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Measurement of muscle tone | Procedure site - Direct (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Myopathic Ehlers-Danlos syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 5 | 
| Congenital myopathy with reduced type 2 muscle fibers | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| X-linked myotubular myopathy, abnormal genitalia syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Administration of inactivated Japanese encephalitis virus adsorbed vaccine via intramuscular route | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Administration of typhoid VI capsular polysaccharide vaccine via intramuscular route | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Administration of rabies vaccine via intramuscular route | Procedure site - Indirect (attribute) | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital contracture of limbs and face, hypotonia, developmental delay syndrome | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 6 | 
| Antenatal multi-minicore disease with arthrogryposis multiplex congenita | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Congenital multi-minicore disease with external ophthalmoplegia (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Pain in multiple muscles | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Inflammation of multiple muscles | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Disorder of skeletal muscle due to systemic sclerosis (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Andersen Tawil syndrome (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Combined oxidative phosphorylation defect type 39 | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Laminin alpha-2 related limb girdle muscular dystrophy R23 (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| Calpain-3-related limb girdle muscular dystrophy D4 | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 1 | 
| G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Upper limb spasticity after stroke (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Spasticity in wrist and hand after stroke (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Spasticity in multiple sclerosis (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Severe chronic spasticity (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Chronic spasticity (finding) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 2 | 
| Spasticity in ankle joint after stroke | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 3 | 
| Huntington's chorea with hyperactive behavior (disorder) | Finding site | True | Skeletal muscle structure | Inferred relationship | Some | 5 |