CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC
disease
Disease or Syndrome
1
2
0.600
None
0
2
Amyotrophic Lateral Sclerosis
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
1114
485
0.500
None
1.000
20
1
1993
2018
Amyotrophic Lateral Sclerosis, Familial
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
130
68
0.310
None
1.000
1
1996
1996
Peripheral Nervous System Diseases
group
Nervous System Diseases
Disease or Syndrome
549
69
0.300
None
1.000
1
1999
1999
Amyotrophic Lateral Sclerosis, Sporadic
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
173
90
0.300
None
0
AMYOTROPHIC LATERAL SCLEROSIS 1
disease
Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
164
139
0.300
None
0
Sciatic Neuropathy
disease
Nervous System Diseases
Disease or Syndrome
115
0.200
None
1.000
2
1988
2002
Transient Ischemic Attack
disease
Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
344
16
0.200
None
1.000
1
1996
1996
Hypothyroidism
disease
Endocrine System Diseases
Disease or Syndrome
613
283
0.200
None
1.000
1
1999
1999
Phenylketonuria, Maternal
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases
Disease or Syndrome
6
2
0.200
None
1.000
1
1993
1993
Wallerian Degeneration
phenotype
Pathological Conditions, Signs and Symptoms
Cell or Molecular Dysfunction
21
0.200
None
1.000
1
2000
2000
Congenital Hypothyroidism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
Disease or Syndrome
94
48
0.200
None
1.000
1
2008
2008
Diabetes Mellitus, Experimental
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Experimental Model of Disease
522
0.200
None
1.000
1
2003
2003
Endemic Cretinism
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
Disease or Syndrome
26
0.200
None
1.000
1
2008
2008
Phenylketonurias
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
83
46
0.200
None
1.000
1
1993
1993
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.110
None
< 0.001
1
2018
2018
Generalized muscle weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
126
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
Agitation
phenotype
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Sign or Symptom
109
4
0.100
None
0
Increased variability in muscle fiber diameter
phenotype
Finding
50
4
0.100
None
0
Xerostomia
disease
Stomatognathic Diseases
Finding
56
1
0.100
None
0
Degeneration of the lateral corticospinal tracts
phenotype
Finding
21
0.100
None
0
Distal sensory impairment
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
86
5
0.100
None
0
Sleep Apnea Syndromes
disease
Respiratory Tract Diseases; Nervous System Diseases
Disease or Syndrome
148
18
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