MB, myoglobin, 4151

N. diseases: 125; N. variants: 2
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: C0010392
Disease: Crush syndrome
Crush syndrome 		phenotype Wounds and Injuries Pathologic Function 1 0.200 None 1.000 1 2003 2003
CUI: C0410257
Disease: Traumatic rhabdomyolysis
Traumatic rhabdomyolysis 		disease Musculoskeletal Diseases Disease or Syndrome 1 1 0.010 None 1.000 1 2017 2017
CUI: C0858572
Disease: Rigidity of limbs
Rigidity of limbs 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C1112262
Disease: Tissue anoxia
Tissue anoxia 		phenotype Sign or Symptom 1 0.010 None 1.000 1 2018 2018
CUI: C1142397
Disease: Myoglobinaemia
Myoglobinaemia 		disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0267964
Disease: Pancreatic acinar atrophy
Pancreatic acinar atrophy 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 3 0.010 None < 0.001 1 2019 2019
CUI: C0009492
Disease: Compartment syndromes
Compartment syndromes 		group Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 4 0.030 None 1.000 3 2017 2019
CUI: C1720775
Disease: Renal tubular necrosis
Renal tubular necrosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 9 0.010 None 1.000 1 2005 2005
CUI: C0342790
Disease: Carnitine palmitoyl transferase 2 deficiency
Carnitine palmitoyl transferase 2 deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 11 29 0.010 None 1.000 1 2005 2005
CUI: C1456624
Disease: Methamphetamine abuse
Methamphetamine abuse 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 15 4 0.010 None 1.000 1 2018 2018
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 18 10 0.010 None 1.000 1 1985 1985
CUI: C0017924
Disease: Glycogen Storage Disease Type V
Glycogen Storage Disease Type V 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 22 76 0.010 None 1.000 1 2018 2018
CUI: C3267003
Disease: Vascular endothelial growth factor overexpression
Vascular endothelial growth factor overexpression 		disease Disease or Syndrome 26 0.010 None 1.000 1 2004 2004
CUI: C0151814
Disease: Coronary Occlusion
Coronary Occlusion 		disease Cardiovascular Diseases Disease or Syndrome 28 1 0.010 None 1.000 1 2019 2019
CUI: C1442837
Disease: Myocardial necrosis
Myocardial necrosis 		disease Cardiovascular Diseases Disease or Syndrome 30 2 0.010 None 1.000 1 2018 2018
CUI: C0410174
Disease: Fukuyama Type Congenital Muscular Dystrophy
Fukuyama Type Congenital Muscular Dystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases Disease or Syndrome 35 29 0.010 None 1.000 1 2012 2012
CUI: C0029438
Disease: Massive Osteolyses
Massive Osteolyses 		disease Musculoskeletal Diseases Disease or Syndrome 44 11 0.010 None 1.000 1 2018 2018
CUI: C0334287
Disease: Fibrolamellar Hepatocellular Carcinoma
Fibrolamellar Hepatocellular Carcinoma 		disease Digestive System Diseases; Neoplasms Neoplastic Process 46 0.010 None 1.000 1 2017 2017
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 47 3 0.010 None 1.000 1 2016 2016
CUI: C0022672
Disease: Acute Kidney Tubular Necrosis
Acute Kidney Tubular Necrosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 53 0.030 None 1.000 3 2013 2018
CUI: C0234233
Disease: Sore to touch
Sore to touch 		phenotype Pathological Conditions, Signs and Symptoms; Mental Disorders Sign or Symptom 56 8 0.020 None 1.000 2 2008 2018
CUI: C0017495
Disease: Gerstmann-Straussler-Scheinker Disease
Gerstmann-Straussler-Scheinker Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases Disease or Syndrome 56 39 0.010 None 1.000 1 2018 2018
CUI: C4082974
Disease: Dupuytren's Disease
Dupuytren's Disease 		disease Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 59 14 0.020 None 1.000 2 2008 2011
CUI: C0242184
Disease: Hypoxia
Hypoxia 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 59 0.200 None 1.000 1 2002 2002
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 63 16 0.010 None 1.000 1 2018 2018