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: 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: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.010 None 1.000 1 2017 2017
CUI: C0281902
Disease: maladjustment
maladjustment
phenotype Mental or Behavioral Dysfunction 13 0.010 None 1.000 1 2005 2005
CUI: C0278134
Disease: Absence of sensation
Absence of sensation
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 111 5 0.010 None 1.000 1 2019 2019
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
disease Disease or Syndrome 695 94 0.010 None 1.000 1 1993 1993
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: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
disease Cardiovascular Diseases Disease or Syndrome 756 103 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: C0264789
Disease: Familial cardiomyopathy
Familial cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2018 2018
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 104 31 0.010 None 1.000 1 2014 2014
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 274 83 0.010 None < 0.001 1 2007 2007
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4388 1168 0.010 None 1.000 1 2017 2017
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
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.010 None 1.000 1 1993 1993
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
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: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
disease Respiratory Tract Diseases Disease or Syndrome 803 63 0.010 None 1.000 1 2010 2010
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
Takotsubo Cardiomyopathy
disease Cardiovascular Diseases Disease or Syndrome 44 3 0.010 None 1.000 1 2017 2017
CUI: C1397307
Disease: Cardiac fibrosis
Cardiac fibrosis
disease Disease or Syndrome 297 3 0.010 None 1.000 1 2014 2014
Adenocarcinoma of the gastroesophageal junction
disease Digestive System Diseases; Neoplasms Neoplastic Process 32 6 0.010 None 1.000 1 2017 2017
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: C0860659
Disease: Aloof
Aloof
disease Mental or Behavioral Dysfunction 81 0.010 None 1.000 1 2017 2017
CUI: C0856742
Disease: Post MI
Post MI
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 203 4 0.010 None 1.000 1 2018 2018
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 201 661 0.010 None 1.000 1 2010 2010