TMEM43, transmembrane protein 43, 79188

N. diseases: 38; N. variants: 5
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.
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)
disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 3 1 0.600 4 1 2008 2017
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 8 70 0.500 0
Arrhythmogenic Right Ventricular Dysplasia
disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality; Disease or Syndrome 41 107 0.480 strong 1.000 9 2 2008 2016
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
phenotype Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms Pathologic Function 49 2 0.400 1 2010 2010
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT
disease Disease or Syndrome 1 2 0.400 1 2 2011 2011
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 32 12 0.320 1.000 2 2011 2015
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
group Cardiovascular Diseases Disease or Syndrome 418 387 0.310 limited 1.000 1 1 2015 2015
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest
phenotype Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms Pathologic Function 20 30 0.300 1 2010 2010
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
disease Digestive System Diseases Experimental Model of Disease 800 0.300 1 2015 2015
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart
group Cardiovascular Diseases Disease or Syndrome 78 0.300 limited 0
Congenital muscular dystrophy (disorder)
disease Disease or Syndrome 66 10 0.300 limited 0
X-Linked Emery-Dreifuss Muscular Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 29 10 0.300 0
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 5 3 0.300 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 306 6 0.300 limited 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 297 104 0.300 limited 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
group Cardiovascular Diseases Disease or Syndrome 479 108 0.110 1.000 1 1 2013 2013
CUI: C0151636
Disease: Premature ventricular contractions
Premature ventricular contractions
phenotype Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 9 1 0.100 0
CUI: C0018801
Disease: Heart failure
Heart failure
disease Cardiovascular Diseases Disease or Syndrome 814 91 0.100 0
CUI: C0008031
Disease: Chest Pain
Chest Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 75 2 0.100 0
CUI: C1838869
Disease: Proximal neurogenic muscle weakness
Proximal neurogenic muscle weakness
phenotype Sign or Symptom 70 2 0.100 0
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy
disease Disease or Syndrome 18 1 0.100 0
Muscle biopsy shows dystrophic changes
phenotype Finding 63 9 0.100 0
CUI: C2063326
Disease: Right ventricular cardiomyopathy
Right ventricular cardiomyopathy
disease Disease or Syndrome 10 1 0.100 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
disease Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 287 216 0.100 0
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease Cardiovascular Diseases Disease or Syndrome 883 65 0.100 0