Fibrosis, Liver
disease
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
Disease or Syndrome
1179
64
0.010
None
1.000
1
2013
2013
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2017
2017
Nicotine Dependence
disease
Chemically-Induced Disorders; Mental Disorders
Mental or Behavioral Dysfunction
170
178
0.010
None
1.000
1
2011
2011
Hereditary Motor and Sensory Neuropathies
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
53
11
0.010
None
1.000
1
2020
2020
Neuralgia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
767
16
0.010
None
1.000
1
2017
2017
Hearing complaints (excluding H84-86)
phenotype
Sign or Symptom
1
0.010
None
1.000
1
2019
2019
Mood Disorders
group
Mental Disorders
Mental or Behavioral Dysfunction
580
308
0.010
None
1.000
1
2018
2018
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.010
None
1.000
1
2011
2011
Sensorimotor neuropathy
disease
Disease or Syndrome
93
21
0.010
None
1.000
1
2018
2018
Peripheral Neuropathy
group
Nervous System Diseases
Disease or Syndrome
351
81
0.010
None
1.000
1
2016
2016
Congenital deafness
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Nervous System Diseases; Otorhinolaryngologic Diseases
Congenital Abnormality
72
11
0.010
None
1.000
1
2018
2018
Abnormal behavior
phenotype
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
910
121
0.010
None
1.000
1
2017
2017
Depressed mood
phenotype
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
1461
269
0.010
None
1.000
1
2017
2017
Hereditary Motor and Sensory-Neuropathy Type II
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
48
144
0.010
None
1.000
1
2020
2020
Agenesis of corpus callosum
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Congenital Abnormality
615
45
0.010
None
1.000
1
2016
2016
Epstein-Barr Virus Infections
group
Infections
Disease or Syndrome
384
72
0.010
None
1.000
1
2011
2011
Vertigo
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
Sign or Symptom
173
35
0.010
None
1.000
1
2019
2019
Impaired cognition
disease
Mental Disorders
Mental or Behavioral Dysfunction
1630
348
0.010
None
1.000
1
2018
2018
×
CUI:
C0338831
Disease:
Manic
Manic
disease
Mental Disorders
Mental or Behavioral Dysfunction
166
8
0.010
None
1.000
1
2018
2018
melanoma
disease
Neoplasms
Neoplastic Process
3087
515
0.010
None
1.000
1
2017
2017
Peripheral axonal neuropathy
disease
Nervous System Diseases
Disease or Syndrome
94
12
0.010
None
1.000
1
2016
2016
Down Syndrome
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Disease or Syndrome
766
80
0.010
None
1.000
1
2001
2001
Dizziness
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
64
14
0.010
None
1.000
1
2019
2019
Depressive disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
1719
297
0.010
None
1.000
1
2017
2017
Mental Depression
disease
Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
1478
271
0.010
None
1.000
1
2017
2017