Xerostomia
disease
Stomatognathic Diseases
Finding
56
1
0.100
None
0
Dyspnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
222
26
0.100
None
0
Pseudobulbar Palsy
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
13
0.100
None
0
Sleep Apnea Syndromes
disease
Respiratory Tract Diseases; Nervous System Diseases
Disease or Syndrome
148
18
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
Generalized muscle weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
126
4
0.100
None
0
Nausea and vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
257
11
0.100
None
0
Agitation, CTCAE 3.0
phenotype
Finding
87
0.100
None
0
Laryngospasm
disease
Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
48
0.100
None
0
Degeneration of anterior horn cells
phenotype
Nervous System Diseases
Finding
15
0.100
None
0
Fatigable weakness of respiratory muscles
phenotype
Finding
60
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
Agitation, CTCAE 5.0
phenotype
Finding
87
0.100
None
0
Generalized Muscle Weakness, CTCAE
phenotype
Finding
117
0.100
None
0
Degeneration of the lateral corticospinal tracts
phenotype
Finding
21
0.100
None
0
Agitation
phenotype
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Sign or Symptom
109
4
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
Hyperreflexia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
539
19
0.100
None
0
AMYOTROPHIC LATERAL SCLEROSIS 1
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
164
139
1.000
strong
0.980
294
46
1976
2019
HMN (Hereditary Motor Neuropathy) Proximal Type I
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
34
8
0.020
None
1.000
2
1976
1982
Hartnup Disease
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
Disease or Syndrome
12
16
0.010
None
1.000
1
1976
1976
Down Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
766
80
0.400
None
1.000
48
1977
2017
Complete Trisomy 21 Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
669
77
0.100
None
1.000
40
1980
2017