Myocardial Ischemia
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
756
|
103
|
0.300 |
None |
1.000 |
1 |
|
2000 |
2000 |
Chronic Airflow Obstruction
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
35
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Other restrictive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
5
|
|
0.300 |
None |
1.000 |
1 |
|
2006 |
2006 |
Adult Glycogen Storage Disease Type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Ventricular Dysfunction, Left
|
phenotype |
Cardiovascular Diseases
|
Pathologic Function
|
88
|
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Generalized glycogen storage disease of infants
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
51
|
16
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Sudden Cardiac Death
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
133
|
40
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Sudden Cardiac Arrest
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
27
|
32
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Cardiovascular Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
1756
|
711
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Glycogen storage disease type II
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
194
|
269
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Heart Diseases
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
537
|
45
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Cardiac Hypertrophy
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
88
|
11
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Necrosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Organ or Tissue Function
|
60
|
|
0.300 |
None |
1.000 |
1 |
|
2007 |
2007 |
Tachycardia, Ventricular
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
104
|
31
|
0.300 |
None |
1.000 |
1 |
|
2003 |
2003 |
Respiratory Distress Syndrome, Newborn
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Disease or Syndrome
|
177
|
37
|
0.300 |
None |
1.000 |
1 |
|
2000 |
2000 |
Glycogen Storage Disease Type II, Juvenile
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.300 |
None |
1.000 |
1 |
|
2016 |
2016 |
Restrictive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
30
|
0.110 |
None |
1.000 |
2 |
4
|
1999 |
2006 |
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
9
|
163
|
0.100 |
None |
1.000 |
8 |
1
|
1997 |
2015 |
Triglycerides measurement
|
phenotype |
|
Laboratory Procedure
|
563
|
1418
|
0.100 |
None |
1.000 |
1 |
1
|
2012 |
2012 |
Cardiac troponin T measurement
|
phenotype |
|
Laboratory Procedure
|
11
|
19
|
0.100 |
None |
1.000 |
1 |
2
|
2013 |
2013 |
Lipoatrophy
|
disease |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
106
|
6
|
0.100 |
None |
|
0 |
|
|
|
Electromyogram abnormal
|
phenotype |
|
Finding
|
130
|
12
|
0.100 |
None |
|
0 |
|
|
|
Neutrophil abnormality
|
phenotype |
|
Finding
|
74
|
1
|
0.100 |
None |
|
0 |
|
|
|
Keratoderma, Palmoplantar
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
165
|
19
|
0.100 |
None |
|
0 |
|
|
|
Sensorineural Hearing Loss (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
783
|
111
|
0.100 |
None |
|
0 |
|
|
|