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 |