Generalized Muscle Weakness, CTCAE
phenotype
Finding
117
0.100
None
0
Xerostomia
disease
Stomatognathic Diseases
Finding
56
1
0.100
None
0
×
CUI:
C0037763
Disease:
Spasm
Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
172
9
0.100
None
0
Dyspnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
222
26
0.100
None
0
Fatigue
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
760
67
0.100
None
0
Agitation, CTCAE 3.0
phenotype
Finding
87
0.100
None
0
Respiratory Failure
disease
Respiratory Tract Diseases
Disease or Syndrome
319
23
0.100
None
0
Nerve Degeneration
phenotype
Pathological Conditions, Signs and Symptoms
Cell or Molecular Dysfunction
165
17
0.100
None
0
Laryngospasm
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
48
0.100
None
0
Nausea and vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
257
11
0.100
None
0
Agitation
phenotype
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Sign or Symptom
109
4
0.100
None
0
Mood swings
disease
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
171
1
0.100
None
0
Generalized muscle weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
126
4
0.100
None
0
Agitation, CTCAE 5.0
phenotype
Finding
87
0.100
None
0
Paralysed
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
68
0.100
None
0
Skeletal muscle atrophy
phenotype
Pathologic Function
306
12
0.100
None
0
Muscle Spasticity
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
580
48
0.100
None
0
Fatigable weakness of swallowing muscles
phenotype
Finding
39
0.100
None
0
Spasticity, CTCAE
phenotype
Finding
477
0.100
None
0
Fatigable weakness of respiratory muscles
phenotype
Finding
60
0.100
None
0
Primary hyperoxaluria, type I
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
27
169
0.010
None
1.000
1
1989
1989
Bipolar I disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
83
46
0.310
None
1.000
1
2005
2005
Depressive Symptoms
phenotype
Behavior and Behavior Mechanisms
Sign or Symptom
421
120
0.310
None
1.000
1
2007
2007
Mood Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
580
308
0.310
None
1.000
1
2007
2007
Autistic Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1112
395
0.300
None
1.000
1
2007
2007