EDN1, endothelin 1, 1906

N. diseases: 679; N. variants: 23
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: C4749274
Disease: Chuvash erythrocytosis
Chuvash erythrocytosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 17 2 0.010 None 1.000 1 2006 2006
CUI: C0878552
Disease: Coronary artery ectasia
Coronary artery ectasia
disease Disease or Syndrome 24 1 0.010 None 1.000 1 2017 2017
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 144 114 0.010 None 1.000 1 2004 2004
CUI: C1096458
Disease: Vascular occlusion
Vascular occlusion
disease Cardiovascular Diseases Disease or Syndrome 30 2 0.010 None 1.000 1 2017 2017
CUI: C1135194
Disease: Chronic systolic heart failure
Chronic systolic heart failure
disease Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C0022679
Disease: Cystic kidney
Cystic kidney
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 89 1 0.010 None 1.000 1 2003 2003
CUI: C1153706
Disease: Endometrial adenocarcinoma
Endometrial adenocarcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 212 5 0.010 None 1.000 1 1992 1992
CUI: C0752130
Disease: Spinal Cord Ischemia
Spinal Cord Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 35 3 0.010 None 1.000 1 2019 2019
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 102 4 0.010 None 1.000 1 1995 1995
CUI: C0025209
Disease: Melanosis
Melanosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 26 23 0.010 None 1.000 1 1996 1996
CUI: C0027796
Disease: Neuralgia
Neuralgia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 767 16 0.010 None 1.000 1 2018 2018
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 384 45 0.010 None 1.000 1 2014 2014
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 196 76 0.010 None 1.000 1 2017 2017
CUI: C0741281
Disease: atrial fibrillation new onset
atrial fibrillation new onset
disease Disease or Syndrome 18 0.010 None 1.000 1 2019 2019
CUI: C0741923
Disease: cardiac event
cardiac event
phenotype Disease or Syndrome 82 18 0.010 None 1.000 1 2011 2011
CUI: C0027543
Disease: Avascular necrosis of bone
Avascular necrosis of bone
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 73 5 0.010 None 1.000 1 2018 2018
CUI: C0027059
Disease: Myocarditis
Myocarditis
disease Cardiovascular Diseases Disease or Syndrome 285 2 0.010 None 1.000 1 2005 2005
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 2005 2005
CUI: C0745130
Disease: Resistant hypertensive disorder
Resistant hypertensive disorder
disease Cardiovascular Diseases Disease or Syndrome 47 14 0.010 None 1.000 1 2017 2017
CUI: C0750151
Disease: Vaso-Occlusive Crisis
Vaso-Occlusive Crisis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 30 5 0.010 None 1.000 1 2003 2003
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 1740 865 0.010 None 1.000 1 2017 2017
CUI: C0026265
Disease: Diseases of mitral valve
Diseases of mitral valve
group Cardiovascular Diseases Disease or Syndrome 21 2 0.010 None 1.000 1 2018 2018
CUI: C0750927
Disease: Apraxia, Developmental Verbal
Apraxia, Developmental Verbal
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 80 21 0.010 None 1.000 1 2019 2019
Hyperphenylalaninemia, Non-Phenylketonuric
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2003 2003
CUI: C0751674
Disease: Lymphangioleiomyomatosis
Lymphangioleiomyomatosis
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 96 17 0.010 None 1.000 1 2018 2018