| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Nemaline myopathy, late onset type |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Actin accumulation myopathy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Typical nemaline myopathy |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Childhood-onset nemaline myopathy |
Interprets |
True |
Movement |
Inferred relationship |
Some |
3 |
| Amish nemaline myopathy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Intermediate nemaline myopathy |
Interprets |
True |
Movement |
Inferred relationship |
Some |
3 |
| Severe congenital nemaline myopathy |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome |
Interprets |
False |
Movement |
Inferred relationship |
Some |
5 |
| Acute paraparesis (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
5 |
| Acute flaccid paraparesis (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
6 |
| Hemiparesis due to cerebrovascular accident (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Left-sided horizontal gaze palsy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
3 |
| Right-sided horizontal gaze palsy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
3 |
| Hypertonic hemiplegia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
3 |
| Congenital hemiplegia (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Spastic paraplegia associated with human T-cell lymphotropic virus 1 infection (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
6 |
| Quadriparetic cerebral palsy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
7 |
| Classic progressive supranuclear palsy syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
5 |
| Spastic quadriparesis (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
6 |
| Adult familial nephronophthisis with spastic quadriparesia syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
7 |
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome |
Interprets |
True |
Movement |
Inferred relationship |
Some |
7 |
| Tetraparesis |
Interprets |
True |
Movement |
Inferred relationship |
Some |
5 |
| Early-onset myopathy, areflexia, respiratory distress, dysphagia syndrome (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) |
Interprets |
False |
Movement |
Inferred relationship |
Some |
11 |
| Myosin storage myopathy (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
2 |
| Weakness of right facial muscle due to and following non-traumatic intracranial subarachnoid hemorrhage |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Weakness of left facial muscle due to and following non-traumatic intracranial subarachnoid haemorrhage |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Weakness of facial muscle as a sequela of haemorrhagic cerebrovascular accident |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Weakness of facial muscle due to and following non-traumatic intracranial subarachnoid hemorrhage (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
4 |
| Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
6 |
| X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) |
Interprets |
True |
Movement |
Inferred relationship |
Some |
13 |