Mitochondrial Diseases
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
284
|
84
|
0.310 |
strong |
1.000 |
2 |
|
2016 |
2018 |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
|
disease |
|
Disease or Syndrome
|
2
|
13
|
0.300 |
strong |
|
0 |
|
|
|
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Leigh Syndrome due to Mitochondrial Complex V Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
40
|
8
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Necrotizing encephalopathy, infantile subacute, of Leigh
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Leigh Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
144
|
114
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
37
|
12
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
36
|
1
|
0.300 |
definitive |
1.000 |
8 |
|
2011 |
2018 |
Ubiquinone dehydrogenase deficiency
|
disease |
|
Disease or Syndrome
|
10
|
2
|
0.040 |
None |
1.000 |
4 |
|
2013 |
2017 |
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
10
|
1
|
0.530 |
None |
1.000 |
3 |
|
2011 |
2018 |
Neurodegenerative Disorders
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
1515
|
85
|
0.320 |
None |
1.000 |
3 |
|
2011 |
2015 |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
|
disease |
|
Disease or Syndrome
|
1
|
6
|
0.400 |
None |
1.000 |
2 |
6
|
2011 |
2016 |
Body mass index
|
phenotype |
|
Clinical Attribute
|
1014
|
2689
|
0.100 |
None |
1.000 |
2 |
1
|
2019 |
2019 |
Encephalopathies
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
457
|
64
|
0.020 |
None |
1.000 |
2 |
|
2011 |
2018 |
nervous system disorder
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
977
|
39
|
0.310 |
None |
1.000 |
2 |
|
2011 |
2015 |
Gait, Drop Foot
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
51
|
5
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Marche a Petit Pas
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Rapid Fatigue of Gait
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Gait, Stumbling
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Sign or Symptom
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Sterility, Reproductive
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Pathologic Function
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Degenerative Diseases, Central Nervous System
|
group |
Nervous System Diseases
|
Disease or Syndrome
|
43
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Gait, Broadened
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Gait, Hysterical
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Gait, Hemiplegic
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Finding
|
4
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |