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 |