| 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 |