Thyrotoxic periodic paralysis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
15
|
32
|
0.320 |
None |
1.000 |
3 |
|
2003 |
2007 |
Central Core Myopathy (disorder)
|
disease |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
44
|
110
|
0.020 |
None |
1.000 |
2 |
|
2006 |
2011 |
Hereditary pyropoikilocytosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
47
|
23
|
0.020 |
None |
1.000 |
2 |
|
2012 |
2015 |
Congenital myopathy (disorder)
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Congenital Abnormality
|
63
|
10
|
0.320 |
strong |
1.000 |
2 |
|
2017 |
2018 |
Myasthenia Gravis
|
disease |
Neoplasms; Immune System Diseases; Nervous System Diseases
|
Disease or Syndrome
|
336
|
93
|
0.010 |
None |
1.000 |
1 |
|
2014 |
2014 |
Metabolic myopathy
|
group |
Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
18
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
|
disease |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
Disease or Syndrome
|
31
|
121
|
0.010 |
None |
1.000 |
1 |
|
2011 |
2011 |
Purpura, Thrombotic Thrombocytopenic
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
80
|
13
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Amyotrophic Lateral Sclerosis
|
disease |
Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
1114
|
485
|
0.010 |
None |
1.000 |
1 |
|
2008 |
2008 |
Liver carcinoma
|
disease |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
5725
|
942
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Respiratory Insufficiency
|
phenotype |
Respiratory Tract Diseases
|
Pathologic Function
|
315
|
15
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Periodic paralysis with transient compartment-like syndrome
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
1
|
|
0.300 |
None |
1.000 |
1 |
|
2013 |
2013 |
Respiratory Failure
|
disease |
Respiratory Tract Diseases
|
Disease or Syndrome
|
319
|
23
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Congenital Thrombotic Thrombocytopenic Purpura
|
disease |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
|
Disease or Syndrome
|
36
|
66
|
0.010 |
None |
1.000 |
1 |
|
2007 |
2007 |
Gastric Cardia Adenocarcinoma
|
disease |
|
Neoplastic Process
|
65
|
11
|
0.010 |
None |
1.000 |
1 |
|
2016 |
2016 |
RETINITIS PIGMENTOSA 12 (disorder)
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
3
|
38
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Andersen Syndrome
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Disease or Syndrome
|
23
|
38
|
0.010 |
None |
1.000 |
1 |
|
2018 |
2018 |
Intraocular pressure disorder
|
disease |
Eye Diseases
|
Disease or Syndrome
|
304
|
56
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Liver neoplasms
|
group |
Digestive System Diseases; Neoplasms
|
Neoplastic Process
|
1424
|
7
|
0.010 |
None |
1.000 |
1 |
|
1997 |
1997 |
Rheumatoid Arthritis
|
disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
|
Disease or Syndrome
|
2723
|
2387
|
0.010 |
None |
1.000 |
1 |
|
2009 |
2009 |
Respiratory Depression
|
phenotype |
Respiratory Tract Diseases
|
Pathologic Function
|
24
|
5
|
0.300 |
None |
1.000 |
1 |
|
2010 |
2010 |
Neuromuscular inhibition
|
disease |
|
Disease or Syndrome
|
72
|
2
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |
Epilepsy
|
disease |
Nervous System Diseases
|
Disease or Syndrome
|
1215
|
339
|
0.010 |
None |
1.000 |
1 |
|
2000 |
2000 |
Retinitis Pigmentosa
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
|
Disease or Syndrome
|
546
|
541
|
0.010 |
None |
1.000 |
1 |
|
1996 |
1996 |
Normokalemic Periodic Paralysis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
|
Disease or Syndrome
|
2
|
3
|
0.010 |
None |
1.000 |
1 |
|
2017 |
2017 |