Fetal Growth Retardation
phenotype
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Disease or Syndrome
1037
21
0.010
None
1.000
1
2017
2017
Edema of foot (finding)
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
19
0.010
None
1.000
1
2019
2019
Shigella Infections
group
Digestive System Diseases; Infections
Disease or Syndrome
121
0.010
None
1.000
1
2018
2018
Crohn Disease
disease
Digestive System Diseases
Disease or Syndrome
1382
1147
0.010
None
1.000
1
2017
2017
×
CUI:
C0030193
Disease:
Pain
Pain
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
1554
196
0.010
None
1.000
1
2020
2020
Ulcerative Colitis
disease
Digestive System Diseases
Disease or Syndrome
1458
827
0.010
None
1.000
1
2017
2017
Septicemia
disease
Pathological Conditions, Signs and Symptoms; Infections
Disease or Syndrome
1285
141
0.010
None
1.000
1
2019
2019
Sepsis
disease
Pathological Conditions, Signs and Symptoms; Infections
Disease or Syndrome
1453
144
0.010
None
1.000
1
2019
2019
Tophus
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Acquired Abnormality
14
3
0.010
None
1.000
1
2019
2019
Arthritis
disease
Musculoskeletal Diseases
Disease or Syndrome
1072
69
0.010
None
1.000
1
2020
2020
Trichohepatoenteric Syndrome
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
Disease or Syndrome
424
28
0.010
None
1.000
1
2019
2019
Cerebrovascular accident
group
Nervous System Diseases; Cardiovascular Diseases
Disease or Syndrome
1658
591
0.020
None
1.000
2
2017
2017
Gout attack
disease
Disease or Syndrome
4
0.020
None
1.000
2
2017
2020
Primary gout
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases
Disease or Syndrome
40
5
0.060
None
1.000
6
2016
2020
Maple syrup urine disease, type 1A
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
1
9
0.100
None
1.000
13
9
1989
2016
Body Height
phenotype
Organism Attribute
1903
3972
0.100
None
1.000
2
2
2014
2019
Red cell distribution width determination
phenotype
Laboratory Procedure
593
988
0.100
None
1.000
1
1
2019
2019
RDW - Red blood cell distribution width result
phenotype
Laboratory or Test Result
593
988
0.100
None
1.000
1
1
2019
2019
Increased level of hippuric acid in urine
phenotype
Finding
7
0.100
None
0
Intellectual Disability
group
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
Mental or Behavioral Dysfunction
2165
159
0.100
None
0
Growth abnormality
phenotype
Finding
49
5
0.100
None
0
MAPLE SYRUP URINE DISEASE, INTERMEDIATE, TYPE IA
phenotype
Finding
1
2
0.100
None
0
2
Feeding difficulties in infancy
phenotype
Finding
305
22
0.100
None
0
Elevated plasma branched chain amino acids
phenotype
Finding
4
0.100
None
0
Generalized hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
955
164
0.100
None
0