Generalized tonic-clonic seizures with focal onset
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
23
1
0.100
None
0
Neonatal Hypotonia
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
169
45
0.100
None
0
Infantile muscular hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
118
24
0.100
None
0
Proteinuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
239
20
0.100
None
0
Status Epilepticus
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
533
12
0.100
None
0
Nephritis, Tubulointerstitial
disease
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
92
6
0.100
None
0
Oligohydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
129
21
0.100
None
0
Undetectable visual evoked potentials
phenotype
Finding
6
1
0.100
None
0
Anasarca
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
41
0.100
None
0
Feeding difficulties
phenotype
Finding
473
62
0.100
None
0
Hypoalbuminemia
disease
Hemic and Lymphatic Diseases
Disease or Syndrome
107
9
0.100
None
0
Severe lactic acidosis
phenotype
Nutritional and Metabolic Diseases
Finding
8
1
0.100
None
0
Episodic vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Finding
43
10
0.100
None
0
Simple renal cyst
disease
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
100
2
0.100
None
0
Developmental regression
disease
Mental Disorders
Disease or Syndrome
333
80
0.100
None
0
Increased serum lactate
phenotype
Nutritional and Metabolic Diseases
Finding
169
2
0.100
None
0
Edema, generalized
phenotype
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
Pathologic Function
12
0.100
None
0
Central visual impairment
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
158
1
0.100
None
0
Renal tubular acidosis
phenotype
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
52
3
0.100
None
0
Generalized Edema, CTCAE
phenotype
Finding
12
0.100
None
0
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0
Cortical visual impairment
phenotype
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Pathologic Function
136
27
0.100
None
0
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
0.100
None
0
Focal T2 hyperintense basal ganglia lesion
phenotype
Finding
46
3
0.100
None
0
Cardiomegaly
phenotype
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
Finding
267
11
0.100
None
0