COENZYME Q10 DEFICIENCY, PRIMARY, 3
disease
Disease or Syndrome
1
3
0.700
None
1.000
4
3
2006
2016
Leigh Disease
disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
Disease or Syndrome
144
114
0.310
strong
1.000
2
2006
2008
Nephrotic Syndrome
group
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Disease or Syndrome
384
45
0.110
None
1.000
1
2018
2018
Parkinson Disease
disease
Nervous System Diseases
Disease or Syndrome
2078
990
0.100
None
1.000
18
2011
2019
Calcification of coronary artery
phenotype
Nutritional and Metabolic Diseases; Cardiovascular Diseases
Pathologic Function
51
205
0.100
None
1.000
1
1
2017
2017
Triglycerides measurement
phenotype
Laboratory Procedure
563
1418
0.100
None
1.000
1
1
2012
2012
Chronic Obstructive Airway Disease
disease
Respiratory Tract Diseases
Disease or Syndrome
1428
852
0.100
None
1.000
1
1
2015
2015
Serum albumin measurement
phenotype
Laboratory Procedure
433
3282
0.100
None
1.000
1
1
2012
2012
Diabetes Mellitus, Non-Insulin-Dependent
disease
Nutritional and Metabolic Diseases; Endocrine System Diseases
Disease or Syndrome
3134
2672
0.100
None
1.000
1
1
2017
2017
Status Epilepticus
disease
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Disease or Syndrome
533
12
0.100
None
0
Undetectable visual evoked potentials
phenotype
Finding
6
1
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
Proteinuria
phenotype
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Finding
239
20
0.100
None
0
Oligohydramnios
phenotype
Female Urogenital Diseases and Pregnancy Complications
Pathologic Function
129
21
0.100
None
0
Infantile muscular hypotonia
phenotype
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
Finding
118
24
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
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
Episodic vomiting
phenotype
Pathological Conditions, Signs and Symptoms
Finding
43
10
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
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
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
×
CUI:
C0013604
Disease:
Edema
Edema
phenotype
Pathological Conditions, Signs and Symptoms
Pathologic Function
126
1
0.100
None
0