| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
4 |
| Pure mitochondrial myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Myofascial pain syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
7 |
| Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Autosomal recessive limb girdle muscular dystrophy type 2T (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| dystrophie musculaire des ceintures autosomique récessive type 2R |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Mitochondrial myopathy, lactic acidosis, deafness syndrome |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
4 |
| Familial infantile myasthenia |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Acetylcholine resynthesis deficiency (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Neuromuscular junction disorder caused by organic phosphorus compound ingestion (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Distal myopathy with posterior leg and anterior hand involvement (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Distal myopathy with posterior leg and anterior hand involvement (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
3 |
| Distal myopathy with early respiratory muscle involvement |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Distal myopathy with early respiratory muscle involvement |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
3 |
| Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Structure of adductor muscle |
Is a |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
|
| Myokymia of left superior oblique muscle (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Myokymia of right superior oblique muscle (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Neuralgic amyotrophy of left brachial plexus (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Neuralgic amyotrophy of right brachial plexus (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Myositis caused by Mycobacterium tuberculosis (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Juvenile polymyositis (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Intermittent claudication |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Venous intermittent claudication |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital muscular dystrophy with hyperlaxity (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital myopathy with myasthenic-like onset (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Lethal congenital contracture syndrome type 5 |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Familial dyskinesia and facial myokymia (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Finnish upper limb onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| KLHL9-related early-onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Oculopharyngodistal myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
4 |
| Menstrual cramp (finding) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Cylindrical spirals myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
3 |
| Laing early-onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital muscular dystrophy type 1B |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital myopathy with internal nuclei and atypical cores (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Muscle filaminopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Myopathy with hexagonally cross-linked tubular arrays |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| King Denborough syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Spheroid body myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| KLHL9-related early-onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Myosclerosis (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Autosomal recessive myogenic arthrogryposis multiplex congenita (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
3 |
| Congenital muscular dystrophy type 1B |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Finnish upper limb onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy with hyperlaxity (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Laing early-onset distal myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Oculopharyngodistal myopathy (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Lethal multiple pterygium syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Distal myotilinopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Intellectual disability, myopathy, short stature, endocrine defect syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Fatal infantile lactic acidosis co-occurrent with methylmalonic aciduria (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Lethal infantile mitochondrial myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Metabolic myopathy due to lactate transporter defect |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Inherited spastic paresis |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Rippling muscle disease with myasthenia gravis (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Late-onset distal myopathy Markesbery Griggs type (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Desmin-related myofibrillar myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Benign Samaritan congenital myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| X-linked parkinsonism with spasticity syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Hereditary inclusion body myopathy type 4 (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Proximal myopathy with extrapyramidal signs |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Distal myopathy with posterior leg and anterior hand involvement (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Adult-onset distal myopathy due to valosin containing protein mutation (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Distal myopathy with early respiratory muscle involvement |
Finding site |
False |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Distal myopathy Welander type (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy due to lamin A/C mutation (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
5 |
| Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Autosomal dominant limb-girdle muscular dystrophy type 1H |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Autosomal recessive lower motor neuron disease with childhood onset |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Deep full thickness burn involving muscle (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Viral myalgia |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Coxsackie muscle infection |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Syphilis of muscle |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Human immunodeficiency virus myopathy |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital muscular dystrophy Paradas type (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Duane anomaly, myopathy, scoliosis syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Intellectual disability, developmental delay, contracture syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Early onset myopathy with fatal cardiomyopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Bethlem myopathy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Puerto Rican infant hypotonia syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Epidermolysis bullosa simplex with muscular dystrophy (disorder) |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Sarcopenia |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
1 |
| Paresis of left lower limb |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Paresis of right lower limb |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |
| Congenital lethal myopathy Compton North type |
Finding site |
True |
Skeletal muscle structure |
Inferred relationship |
Some |
2 |