Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Amyloid myopathy |
Is a |
False |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Rhabdomyolysis |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
A rare hereditary myopathic degeneration of both gastrointestinal and urinary tracts that causes chronic intestinal pseudo-obstruction. It usually presents after the first decade of life with megaduodenum, megacystis and symptoms such as abdominal distension and/or pain, vomiting, constipation, diarrhoea, dysphagia, and/or urinary tract infections. |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Calcification of muscle (disorder) |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Myomalacia |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Muscular dystrophy (disorder) |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
A condition characterized by loss of skeletal muscle mass, primarily in the elderly but can be associated with other conditions that are not exclusively seen in older people. |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hypertrophy. Typically, neck rigidity, rigid spine, Achilles tendon shortening, and respiratory insufficiency later in disease course are present. |
Is a |
False |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Muscle atrophy |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Aicardi's syndrome |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
A rare genetic systemic or rheumatologic disease characterized by infantile onset of skin anomalies (such as delayed wound healing with atrophic scars and mild alopecia with dry and brittle hair), retinal rod degeneration with night blindness, degenerative myopathy with muscle weakness, myalgia, and cramps, osteoarthritis, joint laxity, prolapse of internal organs, floating kidney syndrome, malabsorption syndrome, and hypothyroidism. The phenotype has been reported to be more severe in women than in men. |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
Deposition in skeletal muscle |
Is a |
False |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|
A rare acquired motor neuron disease with characteristics of an initial unilateral weakness in the intrinsic hand muscles that eventually spreads to the opposite limb (with an asymmetrical distribution) and that has a very slow progression of muscular atrophy over a 20 year period. |
Is a |
True |
Degenerative disorder of muscle |
Inferred relationship |
Some |
|