PLN, phospholamban, 5350

N. diseases: 90; N. variants: 6
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1835928
Disease: CARDIOMYOPATHY, DILATED, 1P
CARDIOMYOPATHY, DILATED, 1P 		disease Cardiovascular Diseases Disease or Syndrome 2 4 0.700 strong 1.000 17 4 2003 2019
CUI: C3151265
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18 		disease Disease or Syndrome 2 1 0.600 strong 1.000 4 1 2010 2019
CUI: C0376416
Disease: Hibernation, Myocardial
Hibernation, Myocardial 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 4 0.300 None 1.000 1 2006 2006
CUI: C0206145
Disease: Stunned Myocardium
Stunned Myocardium 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 5 0.300 None 1.000 1 2006 2006
CUI: C1836906
Disease: Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 5 71 0.100 None 0 1
CUI: C0206146
Disease: Myocardial Stunning
Myocardial Stunning 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 6 0.300 None 1.000 1 2006 2006
CUI: C1168330
Disease: Non-ischemic dilated cardiomyopathy
Non-ischemic dilated cardiomyopathy 		disease Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C4025008
Disease: Reduced systolic function
Reduced systolic function 		phenotype Cardiovascular Diseases Finding 8 0.100 None 0
CUI: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2018 2018
CUI: C0281902
Disease: maladjustment
maladjustment 		phenotype Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 2005 2005
CUI: C0344424
Disease: Ventricular Arrhythmia by ECG Finding
Ventricular Arrhythmia by ECG Finding 		phenotype Laboratory or Test Result 17 0.100 None 0
CUI: C1883529
Disease: Ventricular Arrhythmia, CTCAE 3.0
Ventricular Arrhythmia, CTCAE 3.0 		phenotype Finding 17 0.100 None 0
CUI: C4553764
Disease: Ventricular Arrhythmia, CTCAE 5.0
Ventricular Arrhythmia, CTCAE 5.0 		phenotype Finding 17 0.100 None 0
CUI: C0694539
Disease: Chronic atrial fibrillation
Chronic atrial fibrillation 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 31 0.010 None 1.000 1 2018 2018
CUI: C1332166
Disease: Adenocarcinoma of the gastroesophageal junction
Adenocarcinoma of the gastroesophageal junction 		disease Digestive System Diseases; Neoplasms Neoplastic Process 32 6 0.010 None 1.000 1 2017 2017
CUI: C4551854
Disease: HYPOPLASTIC LEFT HEART SYNDROME 1
HYPOPLASTIC LEFT HEART SYNDROME 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 37 12 0.010 None 1.000 1 2014 2014
CUI: C1696708
Disease: Prehypertension
Prehypertension 		disease Cardiovascular Diseases Disease or Syndrome 41 5 0.200 None 1.000 1 2012 2012
CUI: C1844376
Disease: Granulomatous Disease, Chronic, X-Linked
Granulomatous Disease, Chronic, X-Linked 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 42 75 0.010 None 1.000 1 2001 2001
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
Takotsubo Cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 44 3 0.010 None 1.000 1 2017 2017
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 56 13 0.010 None 1.000 1 2018 2018
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 61 24 0.010 None 1.000 1 1996 1996
CUI: C0263630
Disease: Hypertrophic disorder of skin, unspecified
Hypertrophic disorder of skin, unspecified 		group Skin and Connective Tissue Diseases Disease or Syndrome 62 1 0.010 None 1.000 1 2018 2018
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		disease Disease or Syndrome 72 2 0.010 None 1.000 1 2007 2007
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		phenotype Finding 74 1 0.100 None 0
CUI: C1868938
Disease: End stage cardiac failure
End stage cardiac failure 		disease Disease or Syndrome 76 2 0.030 None 1.000 3 1996 2014