Lipodystrophy
|
disease |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
226
|
28
|
0.100 |
None |
|
0 |
|
|
|
Lipoatrophy
|
disease |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
106
|
6
|
0.100 |
None |
|
0 |
|
|
|
Creatine phosphokinase serum increased
|
phenotype |
|
Finding
|
228
|
43
|
0.100 |
None |
|
0 |
|
|
|
Myopathy
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
634
|
166
|
0.100 |
None |
|
0 |
|
|
|
Neutrophil abnormality
|
phenotype |
|
Finding
|
74
|
1
|
0.100 |
None |
|
0 |
|
|
|
Sudden death
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
30
|
3
|
0.100 |
None |
|
0 |
|
|
|
Electromyogram abnormal
|
phenotype |
|
Finding
|
130
|
12
|
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 |
|
|
|
Wolff-Parkinson-White Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
48
|
22
|
0.100 |
None |
|
0 |
1
|
|
|
Keratoderma, Palmoplantar
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
165
|
19
|
0.100 |
None |
|
0 |
|
|
|
Conduction disorder of the heart
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
41
|
11
|
0.010 |
None |
< 0.001 |
1 |
|
2005 |
2005 |
Acute Chest Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
405
|
135
|
0.010 |
None |
< 0.001 |
1 |
|
2015 |
2015 |
Acute Coronary Syndrome
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
440
|
139
|
0.310 |
None |
0.500 |
2 |
|
2005 |
2015 |
Hypertrophic obstructive cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
233
|
90
|
0.400 |
None |
0.923 |
13 |
6
|
1996 |
2016 |
Cardiomyopathy, Familial Idiopathic
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
773
|
243
|
0.400 |
None |
0.944 |
18 |
11
|
2002 |
2017 |
Hypertrophic Cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
560
|
635
|
0.800 |
definitive |
0.982 |
109 |
30
|
1991 |
2018 |
Cardiomyopathy, Familial Hypertrophic, 2
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
30
|
0.900 |
strong |
1.000 |
96 |
30
|
1991 |
2019 |
CARDIOMYOPATHY, DILATED, 1D (disorder)
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
24
|
0.900 |
strong |
1.000 |
95 |
24
|
1991 |
2019 |
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
1
|
21
|
0.600 |
strong |
1.000 |
93 |
21
|
1991 |
2019 |
Cardiomyopathy, Dilated
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
512
|
509
|
0.630 |
None |
1.000 |
42 |
13
|
2000 |
2019 |
Cardiomyopathy, Hypertrophic, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
83
|
355
|
0.500 |
None |
1.000 |
21 |
9
|
1996 |
2006 |
Cardiomyopathies
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
925
|
294
|
0.700 |
None |
1.000 |
15 |
6
|
2004 |
2019 |
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 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.070 |
None |
1.000 |
7 |
|
2004 |
2015 |
Familial dilated cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
83
|
47
|
0.430 |
None |
1.000 |
5 |
3
|
2001 |
2005 |