Global developmental delay
disease
Mental or Behavioral Dysfunction
1825
553
0.100
None
0
Sensorimotor neuropathy
disease
Disease or Syndrome
93
21
0.100
None
0
Aldosterone-Producing Adrenal Cortex Adenoma
disease
Neoplasms; Endocrine System Diseases
Neoplastic Process
2
6
0.100
None
0
3
Hypomagnesemia 2, renal
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
10
1
0.100
None
0
Seizures
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
2152
553
0.310
strong
1.000
2
2018
2020
Hypomagnesemia
phenotype
Nutritional and Metabolic Diseases
Disease or Syndrome
58
11
0.420
strong
1.000
2
2018
2020
Tumor Cell Invasion
phenotype
Neoplastic Process
6626
169
0.020
None
1.000
2
2016
2018
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
2003
2003
Headache
phenotype
Pathological Conditions, Signs and Symptoms
Sign or Symptom
338
75
0.010
None
1.000
1
2005
2005
White Blood Cell Count procedure
phenotype
Laboratory Procedure
681
1322
0.100
None
1.000
1
1
2019
2019
Myocardial Reperfusion Injury
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Pathologic Function
226
0.300
None
1.000
1
2018
2018
Neoplasm Metastasis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6385
327
0.010
None
1.000
1
2018
2018
Nodule
phenotype
Acquired Abnormality
278
19
0.010
None
1.000
1
2016
2016
Paresthesia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
121
8
0.010
None
1.000
1
2005
2005
Carcinogenesis
phenotype
Pathological Conditions, Signs and Symptoms; Neoplasms
Neoplastic Process
6243
355
0.010
None
1.000
1
2018
2018
Endothelial dysfunction
phenotype
Disease or Syndrome
716
25
0.010
None
1.000
1
2007
2007
Hypomagnesemia, CTCAE
phenotype
Finding
21
0.400
strong
1.000
1
2018
2018
Hypokalemia
phenotype
Nutritional and Metabolic Diseases
Finding
61
7
0.100
None
0
Polyuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Sign or Symptom
73
3
0.100
None
0
×
CUI:
C0037763
Disease:
Spasm
Spasm
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Sign or Symptom
172
9
0.100
None
0
Hyporeflexia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
312
0.100
None
0
Absent reflex
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
201
16
0.100
None
0
Hyperactive behavior
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Mental or Behavioral Dysfunction
1263
112
0.100
None
0
Biting self
phenotype
Behavior and Behavior Mechanisms
Finding
4
3
0.100
None
0
Gait, Drop Foot
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
51
5
0.100
None
0