Rippling muscle disease
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
6
|
6
|
0.900 |
None |
1.000 |
31 |
6
|
2001 |
2018 |
LONG QT SYNDROME 9 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
4
|
6
|
0.740 |
limited |
1.000 |
6 |
6
|
2006 |
2018 |
RIPPLING MUSCLE DISEASE 2 (disorder)
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
14
|
0.700 |
None |
1.000 |
26 |
14
|
1998 |
2018 |
Creatine phosphokinase serum increased
|
phenotype |
|
Finding
|
228
|
43
|
0.700 |
None |
1.000 |
5 |
4
|
2000 |
2005 |
MYOPATHY, DISTAL, TATEYAMA TYPE
|
disease |
|
Disease or Syndrome
|
2
|
2
|
0.700 |
None |
1.000 |
3 |
2
|
2002 |
2009 |
Muscular Dystrophies, Limb-Girdle
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
118
|
37
|
0.600 |
strong |
1.000 |
25 |
6
|
1998 |
2016 |
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
9
|
163
|
0.600 |
None |
1.000 |
1 |
1
|
2004 |
2004 |
Sudden infant death syndrome
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
140
|
68
|
0.550 |
None |
1.000 |
5 |
4
|
2007 |
2013 |
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
5
|
5
|
0.400 |
None |
1.000 |
11 |
4
|
2000 |
2019 |
Sudden death
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Pathologic Function
|
30
|
3
|
0.400 |
None |
|
0 |
|
|
|
Cardiomyopathies
|
group |
Cardiovascular Diseases
|
Disease or Syndrome
|
925
|
294
|
0.350 |
None |
1.000 |
5 |
|
2003 |
2016 |
RIPPLING MUSCLE DISEASE 1
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
|
0.310 |
None |
1.000 |
6 |
|
2000 |
2018 |
Cardiomegaly
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Finding
|
267
|
11
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Isolated asymptomatic elevation of creatine phosphokinase
|
phenotype |
Nervous System Diseases
|
Finding
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2000 |
2000 |
Cardiac Hypertrophy
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
88
|
11
|
0.300 |
None |
1.000 |
1 |
|
2009 |
2009 |
Chromosome 3, monosomy 3p25
|
disease |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
3
|
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Congenital Heart Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
406
|
58
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Romano-Ward Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
22
|
17
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Streptozotocin Diabetes
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
112
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Diabetes Mellitus, Experimental
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
522
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Alloxan Diabetes
|
disease |
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
Experimental Model of Disease
|
112
|
|
0.300 |
None |
1.000 |
1 |
|
2008 |
2008 |
Sudden Cardiac Arrest
|
phenotype |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Pathologic Function
|
27
|
32
|
0.300 |
None |
|
0 |
|
|
|
Hypertrophic Cardiomyopathy
|
disease |
Cardiovascular Diseases
|
Disease or Syndrome
|
560
|
635
|
0.240 |
None |
1.000 |
4 |
2
|
2004 |
2011 |
Myocardial Infarction
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
1800
|
680
|
0.210 |
None |
1.000 |
2 |
|
2003 |
2018 |
Cardiomyopathy, Hypertrophic, Familial
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
83
|
355
|
0.210 |
None |
1.000 |
1 |
|
2004 |
2004 |