Venous Thromboembolism
phenotype
Cardiovascular Diseases
Disease or Syndrome
378
408
0.010
None
1.000
1
2018
2018
Tremor
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
528
52
0.100
None
0
Transient hyperphenylalaninemia
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
6
1
0.010
None
1.000
1
1
1997
1997
TOXOPLASMOSIS, CHRONIC
disease
Infections
Disease or Syndrome
6
0.010
None
1.000
1
2015
2015
×
CUI:
C0037763
Disease:
Spasm
Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
172
9
0.010
None
1.000
1
2017
2017
Somnolence
phenotype
Pathological Conditions, Signs and Symptoms
Mental or Behavioral Dysfunction
87
8
0.100
None
0
Small for gestational age fetus
phenotype
Pathological Conditions, Signs and Symptoms
Finding
156
0.100
None
0
Small for gestational age (disorder)
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
Finding
181
34
0.100
None
0
Sialorrhea
disease
Stomatognathic Diseases
Disease or Syndrome
32
1
0.100
None
0
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.100
None
0
Relapsing Fever
disease
Infections
Disease or Syndrome
48
2
0.100
None
0
Recurrent fevers
phenotype
Sign or Symptom
48
4
0.100
None
0
Ptosis
disease
Pathological Conditions, Signs and Symptoms
Disease or Syndrome
607
12
0.100
None
0
Progressive neurologic deterioration
phenotype
Mental Disorders
Finding
33
5
0.100
None
0
Primary Hyperoxaluria
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
16
11
0.010
None
1.000
1
2015
2015
Post-Traumatic Stress Disorder
disease
Mental Disorders
Mental or Behavioral Dysfunction
418
117
0.010
None
1.000
1
2018
2018
Poor suck
phenotype
Finding
103
31
0.100
None
0
Poor head control
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Finding
162
13
0.100
None
0
Phenylketonurias
group
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
83
46
0.030
None
1.000
3
1992
2014
Phenylketonuria II
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
6
16
0.010
None
1.000
1
2017
2017
pathologic fistula
phenotype
Pathological Conditions, Signs and Symptoms
Anatomical Abnormality
71
8
0.010
None
1.000
1
2019
2019
Parkinsonian Disorders
group
Nervous System Diseases
Disease or Syndrome
373
95
0.100
None
0
Pallor
phenotype
Pathological Conditions, Signs and Symptoms
Finding
124
4
0.100
None
0
Opisthotonus
phenotype
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
Sign or Symptom
32
2
0.100
None
0
Oculogyric crisis
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Pathologic Function
9
3
0.100
None
0