Glycogen Storage Disease Type IIb
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
11
|
40
|
1.000 |
definitive |
1.000 |
82 |
38
|
1995 |
2020 |
Cardiomyopathies
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
925
|
294
|
0.500 |
None |
1.000 |
13 |
1
|
2000 |
2019 |
Hypertrophic Cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
560
|
635
|
0.400 |
None |
1.000 |
23 |
9
|
2005 |
2019 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.310 |
None |
1.000 |
2 |
|
2011 |
2014 |
Cardiomyopathy, Hypertrophic, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
83
|
355
|
0.310 |
None |
1.000 |
2 |
2
|
2018 |
2019 |
Glycogen Storage Disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
63
|
16
|
0.310 |
limited |
1.000 |
1 |
|
2005 |
2005 |
Petit mal status
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
78
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Non-Convulsive Status Epilepticus
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
71
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Complex Partial Status Epilepticus
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
68
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Status Epilepticus
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
533
|
12
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Simple Partial Status Epilepticus
|
phenotype |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
68
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Status Epilepticus, Subclinical
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
69
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Grand Mal Status Epilepticus
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases
|
Disease or Syndrome
|
75
|
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Cholestasis
|
disease |
Digestive System Diseases
|
Disease or Syndrome
|
420
|
15
|
0.210 |
None |
1.000 |
1 |
|
2017 |
2017 |
Chronic conjunctivitis
|
disease |
Eye Diseases
|
Disease or Syndrome
|
1
|
|
0.200 |
None |
1.000 |
1 |
|
2018 |
2018 |
Sciatic Neuropathy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
115
|
|
0.200 |
None |
1.000 |
1 |
|
2018 |
2018 |
Delirium, Dementia, Amnestic, Cognitive Disorders
|
group |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
83
|
|
0.200 |
None |
1.000 |
1 |
|
2018 |
2018 |
Intellectual Disability
|
group |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
|
Mental or Behavioral Dysfunction
|
2165
|
159
|
0.150 |
None |
1.000 |
5 |
|
2005 |
2020 |
Cardiac Arrhythmia
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
559
|
111
|
0.110 |
None |
1.000 |
1 |
|
2016 |
2016 |
Impaired cognition
|
disease |
Mental Disorders
|
Mental or Behavioral Dysfunction
|
1630
|
348
|
0.110 |
None |
1.000 |
1 |
|
2017 |
2017 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
512
|
509
|
0.110 |
None |
1.000 |
1 |
2
|
2008 |
2008 |
Wolff-Parkinson-White Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
48
|
22
|
0.110 |
None |
1.000 |
1 |
|
2005 |
2005 |
Hypertrophic obstructive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
233
|
90
|
0.100 |
None |
1.000 |
12 |
|
2005 |
2019 |
Talipes cavus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Anatomical Abnormality
|
213
|
2
|
0.100 |
None |
|
0 |
|
|
|
Creatine phosphokinase serum increased
|
phenotype |
|
Finding
|
228
|
43
|
0.100 |
None |
|
0 |
|
|
|