NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII
|
disease |
|
Disease or Syndrome
|
1
|
3
|
0.700 |
None |
1.000 |
8 |
3
|
2013 |
2017 |
EPISODIC PAIN SYNDROME, FAMILIAL, 3
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
1
|
6
|
0.700 |
None |
1.000 |
7 |
6
|
2013 |
2017 |
Congenital Pain Insensitivity
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
14
|
|
0.530 |
None |
1.000 |
4 |
|
2013 |
2018 |
Hyperalgesia, Thermal
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
154
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Hyperalgesia, Secondary
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
88
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Tactile Allodynia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
114
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Hyperalgesia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
451
|
4
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Hyperalgesia, Primary
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
84
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Mechanical Allodynia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
408
|
4
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Allodynia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
84
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Primary Erythermalgia
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
7
|
14
|
0.300 |
None |
|
0 |
|
|
|
Hereditary Sensory Autonomic Neuropathy, Type 5
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
7
|
5
|
0.300 |
None |
|
0 |
|
|
|
PAROXYSMAL EXTREME PAIN DISORDER
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
13
|
9
|
0.300 |
None |
|
0 |
|
|
|
Sensory Neuropathy, Hereditary
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
19
|
2
|
0.200 |
None |
|
0 |
|
|
|
CUI: |
C0030193 |
Disease: |
Pain
|
Pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
1554
|
196
|
0.170 |
None |
1.000 |
7 |
7
|
2013 |
2017 |
Handedness
|
phenotype |
|
Organism Attribute
|
9
|
14
|
0.100 |
None |
1.000 |
1 |
1
|
2014 |
2014 |
Recurrent respiratory infections
|
phenotype |
Infections; Respiratory Tract Diseases
|
Finding
|
318
|
7
|
0.100 |
None |
|
0 |
|
|
|
Peripheral Nervous System Diseases
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
549
|
69
|
0.100 |
None |
|
0 |
|
|
|
Absence of pain sensation
|
phenotype |
Pathological Conditions, Signs and Symptoms; Mental Disorders
|
Finding
|
14
|
3
|
0.100 |
None |
|
0 |
|
|
|
Clumsiness - motor delay
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Disease or Syndrome
|
393
|
2
|
0.100 |
None |
|
0 |
|
|
|
Abnormal platelets
|
phenotype |
Hemic and Lymphatic Diseases
|
Cell or Molecular Dysfunction
|
11
|
|
0.100 |
None |
|
0 |
|
|
|
Muscle Weakness
|
phenotype |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
|
Sign or Symptom
|
536
|
87
|
0.100 |
None |
|
0 |
|
|
|
Self-Injurious Behavior
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
91
|
9
|
0.100 |
None |
|
0 |
|
|
|
Vasculitis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
294
|
24
|
0.100 |
None |
|
0 |
|
|
|
Erythema
|
phenotype |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
227
|
8
|
0.100 |
None |
|
0 |
|
|
|