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 |
False |
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 |