Sotos' syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
25
|
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Catch - Finding of sensory dimension of pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
8
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Temper tantrum
|
phenotype |
Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
1
|
2
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Memory impairment
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
763
|
48
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Sore to touch
|
phenotype |
Pathological Conditions, Signs and Symptoms; Mental Disorders
|
Sign or Symptom
|
56
|
8
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Mechanical pain
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
30
|
4
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Neurologic Symptoms
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
233
|
30
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Inattention
|
phenotype |
|
Mental or Behavioral Dysfunction
|
66
|
22
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Hyperactive behavior
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Mental or Behavioral Dysfunction
|
1263
|
112
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Gastrointestinal symptom
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
69
|
7
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Penile hypospadias
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Congenital Abnormality
|
127
|
83
|
0.010 |
None |
1.000 |
1 |
|
2003 |
2003 |
ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
|
Disease or Syndrome
|
5
|
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Sclerocornea
|
disease |
Eye Diseases
|
Disease or Syndrome
|
42
|
3
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
Mowat-Wilson syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Disease or Syndrome
|
10
|
93
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Pulmonary Stenosis
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
106
|
40
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Pediatric Obesity
|
disease |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
191
|
67
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Symphysis Pubis Dysfunction
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
23
|
4
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Executive dysfunction
|
disease |
|
Mental or Behavioral Dysfunction
|
33
|
3
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
22q11 Deletion Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
31
|
2
|
0.010 |
None |
1.000 |
1 |
|
2010 |
2010 |
Mechanical Allodynia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
408
|
4
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Glaucoma of childhood
|
disease |
Eye Diseases
|
Disease or Syndrome
|
30
|
15
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
47, XYY syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease or Syndrome
|
9
|
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
Skin Erosion
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
225
|
2
|
0.010 |
None |
< 0.001 |
1 |
|
2017 |
2017 |
Abnormality of the skeletal system
|
disease |
|
Anatomical Abnormality
|
148
|
18
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Primary congenital glaucoma
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
|
Disease or Syndrome
|
24
|
25
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |