Myasthenic Syndromes, Congenital
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
57
40
0.530
strong
1.000
4
1
2016
2019
Neoplasms
group
Neoplasms
Neoplastic Process
10161
1644
0.040
None
1.000
4
2012
2019
Neuropathy, Distal Hereditary Motor, Type VIIA
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
1
1
0.610
None
1.000
3
1
2012
2018
MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC
disease
Disease or Syndrome
1
7
0.600
None
1.000
2
7
2016
2016
Congenital Myasthenic Syndromes, Presynaptic
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
19
0.500
None
1.000
1
2016
2016
Recurrent depression
disease
Mental Disorders
Mental or Behavioral Dysfunction
19
12
0.310
None
1.000
1
1
2008
2008
Depressive Symptoms
phenotype
Behavior and Behavior Mechanisms
Sign or Symptom
421
120
0.310
None
1.000
1
2006
2006
Mood Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
580
308
0.310
None
1.000
1
2013
2013
Distal hereditary motor neuropathy type 7
disease
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Disease or Syndrome
2
0.300
None
1.000
1
2012
2012
Familial infantile myasthenia
disease
Pathological Conditions, Signs and Symptoms; Neoplasms; Respiratory Tract Diseases; Immune System Diseases; Nervous System Diseases
Disease or Syndrome
2
16
0.300
moderate
1.000
1
2016
2016
Unipolar Depression
disease
Mental Disorders
Mental or Behavioral Dysfunction
641
225
0.300
None
1.000
1
2008
2008
Major Depressive Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1236
1451
0.300
None
1.000
1
2008
2008
Graft Rejection
phenotype
Organ or Tissue Function
47
0.200
None
1.000
1
2009
2009
Asthma
disease
Respiratory Tract Diseases; Immune System Diseases
Disease or Syndrome
2096
1536
0.200
None
1.000
1
2007
2007
×
CUI:
C0003578
Disease:
Apnea
Apnea
phenotype
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
Sign or Symptom
262
11
0.110
None
1.000
1
2016
2016
Arthrogryposis
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Disease or Syndrome
198
33
0.110
None
1.000
1
2016
2016
Pancreatitis, Chronic
disease
Digestive System Diseases
Disease or Syndrome
379
56
0.010
None
1.000
1
2017
2017
Luminal A Breast Carcinoma
disease
Neoplastic Process
153
11
0.010
None
1.000
1
2017
2017
Diffuse Large B-Cell Lymphoma
disease
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
Neoplastic Process
1043
127
0.010
None
1.000
1
2019
2019
Gilles de la Tourette syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
Disease or Syndrome
177
63
0.010
None
1.000
1
3
2017
2017
Muscle Weakness
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
536
87
0.010
None
1.000
1
2016
2016
Prostate carcinoma
disease
Neoplasms; Male Urogenital Diseases
Neoplastic Process
4388
1168
0.010
None
1.000
1
2017
2017
Adenocarcinoma of lung (disorder)
disease
Neoplasms
Neoplastic Process
2438
563
0.010
None
1.000
1
2019
2019
Angelman Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
94
135
0.010
None
1.000
1
2010
2010
Inherited neuropathies
disease
Nervous System Diseases
Disease or Syndrome
104
4
0.010
None
1.000
1
1
2019
2019