Malignant hyperpyrexia due to anesthesia
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
60
52
0.080
None
1.000
8
2009
2017
Tubular Aggregate Myopathy
disease
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
67
5
0.320
None
1.000
3
2017
2018
Contracture
disease
Musculoskeletal Diseases
Anatomical Abnormality
111
12
0.030
None
1.000
3
2009
2013
Thyroid associated opthalmopathies
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases
Disease or Syndrome
211
49
0.020
None
0.500
2
2010
2010
Cerebrovascular accident
group
Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
1658
591
0.020
None
1.000
2
2009
2014
Stormorken Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Hemic and Lymphatic Diseases
Disease or Syndrome
3
6
0.010
None
1.000
1
2018
2018
Migraine with Aura
disease
Nervous System Diseases
Disease or Syndrome
87
56
0.010
None
1.000
1
2007
2007
X-linked myopathy with excessive autophagy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
14
9
0.010
None
1.000
1
2014
2014
Impaired glucose tolerance
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
596
81
0.010
None
1.000
1
2004
2004
Common Migraine
disease
Nervous System Diseases
Disease or Syndrome
77
62
0.010
None
1.000
1
2007
2007
orbit (eye disorders)
group
Eye Diseases
Disease or Syndrome
64
0.010
None
1.000
1
2010
2010
Myositis
disease
Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
254
43
0.010
None
1.000
1
2010
2010
Diabetes Mellitus, Experimental
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
522
0.200
None
1.000
1
2002
2002
Vacuolar myopathy
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
16
1
0.010
None
1.000
1
2014
2014
Autoimmune Diseases
group
Immune System Diseases
Disease or Syndrome
1758
428
0.010
None
1.000
1
2010
2010
Muscular Dystrophy, Duchenne
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Disease or Syndrome
375
170
0.010
None
1.000
1
1995
1995
×
CUI:
C0015967
Disease:
Fever
Fever
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1021
66
0.010
None
1.000
1
2017
2017
Increased variability in muscle fiber diameter
phenotype
Finding
50
4
0.100
None
0
Type 2 muscle fiber atrophy
phenotype
Finding
14
2
0.100
None
0
Muscle fiber tubular inclusions
phenotype
Anatomical Abnormality
8
0.100
None
0
EMG: myopathic abnormalities
phenotype
Musculoskeletal Diseases; Nervous System Diseases
Pathologic Function
115
16
0.100
None
0
Centrally nucleated skeletal muscle fibers
phenotype
Finding
25
0.100
None
0
Easy fatigability
phenotype
Finding
74
5
0.100
None
0
Creatine phosphokinase serum increased
phenotype
Finding
228
43
0.100
None
0
Fatiguable weakness of proximal limb muscles
phenotype
Finding
14
0.100
None
0