Myasthenic Syndromes, Congenital
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
57
|
40
|
0.200 |
None |
1.000 |
24 |
5
|
1997 |
2018 |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL
|
disease |
|
Disease or Syndrome
|
2
|
17
|
0.800 |
strong |
1.000 |
14 |
17
|
1995 |
2016 |
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
5
|
21
|
0.900 |
strong |
1.000 |
6 |
18
|
1996 |
2011 |
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL
|
disease |
|
Disease or Syndrome
|
2
|
6
|
0.600 |
strong |
1.000 |
4 |
6
|
1996 |
2012 |
Platelet Count measurement
|
phenotype |
|
Laboratory Procedure
|
265
|
457
|
0.100 |
None |
1.000 |
4 |
4
|
2010 |
2018 |
Myasthenia Gravis
|
disease |
Neoplasms; Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
336
|
93
|
0.040 |
None |
0.750 |
4 |
|
2004 |
2015 |
Blood Protein Measurement
|
phenotype |
|
Laboratory Procedure
|
1156
|
2575
|
0.100 |
None |
1.000 |
2 |
2
|
2018 |
2018 |
Platelet mean volume determination (procedure)
|
phenotype |
|
Laboratory Procedure
|
223
|
371
|
0.100 |
None |
1.000 |
2 |
2
|
2012 |
2016 |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL
|
disease |
|
Disease or Syndrome
|
4
|
8
|
0.300 |
strong |
1.000 |
1 |
|
2011 |
2011 |
Ophthalmoparesis
|
phenotype |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
|
Sign or Symptom
|
61
|
4
|
0.110 |
None |
1.000 |
1 |
|
1999 |
1999 |
Myasthenias
|
disease |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
41
|
3
|
0.110 |
None |
1.000 |
1 |
|
2015 |
2015 |
Platelet Component Distribution Width Measurement
|
phenotype |
|
Laboratory Procedure
|
134
|
200
|
0.100 |
None |
1.000 |
1 |
2
|
2016 |
2016 |
Tonometry
|
phenotype |
|
Diagnostic Procedure
|
206
|
573
|
0.100 |
None |
1.000 |
1 |
1
|
2017 |
2017 |
Impaired ristocetin-induced platelet aggregation
|
phenotype |
|
Pathologic Function
|
6
|
1
|
0.100 |
None |
1.000 |
1 |
1
|
2019 |
2019 |
Thrombocytopenia
|
phenotype |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
592
|
110
|
0.100 |
None |
1.000 |
1 |
3
|
2019 |
2019 |
Hepatitis B
|
disease |
Digestive System Diseases; Infections
|
Disease or Syndrome
|
1449
|
519
|
0.100 |
None |
1.000 |
1 |
1
|
2011 |
2011 |
Macrothrombocytopenia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
34
|
31
|
0.100 |
None |
1.000 |
1 |
2
|
2019 |
2019 |
mathematical ability
|
phenotype |
|
Mental Process
|
854
|
2127
|
0.100 |
None |
1.000 |
1 |
1
|
2018 |
2018 |
Slow channel syndrome
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
6
|
1
|
0.010 |
None |
1.000 |
1 |
1
|
2006 |
2006 |
Malnutrition
|
disease |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
417
|
29
|
0.010 |
None |
1.000 |
1 |
|
2004 |
2004 |
Thymus Hyperplasia
|
disease |
Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
30
|
1
|
0.010 |
None |
1.000 |
1 |
|
2015 |
2015 |
Thymoma
|
disease |
Neoplasms; Hemic and Lymphatic Diseases
|
Neoplastic Process
|
291
|
20
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Hirschsprung Disease
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Disease or Syndrome
|
384
|
162
|
0.010 |
None |
1.000 |
1 |
|
2019 |
2019 |
MYASTHENIA, FAMILIAL INFANTILE, 1
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
|
0 |
|
|
|
Myasthenic Syndrome, Congenital, Fast-Channel
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
Disease or Syndrome
|
3
|
|
0.300 |
None |
|
0 |
|
|
|