Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital myotonia, autosomal recessive form |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Paramyotonia congenita |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Congenital myotonia, autosomal dominant form |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Steinert myotonic dystrophy syndrome |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Infantile myotonia |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Anden specificeret myoton sygdom |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Myoton sygdom, ikke nærmere specificeret |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Congenital myotonic dystrophy |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
Non dystrophic myotonia (disorder) |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Myotonia caused by drug |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Potassium aggravated myotonia (disorder) |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Rippling muscle disease (disorder) |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
A rare myotonic dystrophy of juvenile or adult-onset characterized by mild and fluctuating myotonia, muscle weakness, and rarely cardiac conduction disorders. |
Is a |
False |
Myotonic disorder |
Inferred relationship |
Some |
|
A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia). |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
A rare genetic myotonic syndrome characterized by childhood onset of progressive and severe myotonia (with generalized muscular hypertrophy and progressive impairment of gait) short stature, skeletal abnormalities (including pectus carinatum, short, wedge-shaped thoracolumbar vertebrae, kyphoscoliosis, genu valgum, irregular femoral epiphyses) and mild to moderate intellectual deficiency. Facial dysmorphism and joint limitation are not associated. There have been no further descriptions in the literature since 1984. |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|
Myotonic dystrophy (disorder) |
Is a |
True |
Myotonic disorder |
Inferred relationship |
Some |
|