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: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Acquired Abnormality 1 0.010 None 1.000 1 2005 2005
CUI: C2748545
Disease: QUESTION MARK EARS, ISOLATED
QUESTION MARK EARS, ISOLATED
disease Anatomical Abnormality 1 2 0.410 None 1.000 1 2 2013 2013
CUI: C3810332
Disease: AURICULOCONDYLAR SYNDROME 3
AURICULOCONDYLAR SYNDROME 3
disease Disease or Syndrome 1 2 0.400 None 1.000 1 2 2013 2013
CUI: C4524149
Disease: Complicated atherosclerosis
Complicated atherosclerosis
disease Disease or Syndrome 1 0.010 None 1.000 1 1996 1996
CUI: C0497307
Disease: Feeling depressed
Feeling depressed
phenotype Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C0018022
Disease: Endemic goiter
Endemic goiter
disease Endocrine System Diseases Disease or Syndrome 3 3 0.010 None 1.000 1 2003 2003
CUI: C0024799
Disease: Marginal ulcer
Marginal ulcer
disease Digestive System Diseases Disease or Syndrome 3 0.300 None 1.000 1 2006 2006
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.300 None 1.000 1 2007 2007
Postcapillary pulmonary hypertension
disease Respiratory Tract Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C0399570
Disease: Mandibular condyle aplasia
Mandibular condyle aplasia
phenotype Musculoskeletal Diseases; Stomatognathic Diseases Finding 3 0.100 None 0
CUI: C4021376
Disease: Cleft helix
Cleft helix
phenotype Anatomical Abnormality 3 0.100 None 0
Abnormality of the crus of the helix
phenotype Anatomical Abnormality 3 0.100 None 0
CUI: C1865295
Disease: Auriculo-condylar syndrome
Auriculo-condylar syndrome
disease Otorhinolaryngologic Diseases Disease or Syndrome 4 0.620 moderate 1.000 2 2013 2017
CUI: C4551996
Disease: Auriculocondylar syndrome 1
Auriculocondylar syndrome 1
disease Otorhinolaryngologic Diseases Disease or Syndrome 4 7 0.610 moderate 1.000 2 2013 2018
CUI: C2363915
Disease: Cerebellar ischaemia
Cerebellar ischaemia
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome
disease Disease or Syndrome 4 0.010 None 1.000 1 2020 2020
CUI: C3534591
Disease: Diabetic Heart Disease
Diabetic Heart Disease
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2009 2009
CUI: C4076671
Disease: Prostate cancer metastatic to bone
Prostate cancer metastatic to bone
disease Neoplastic Process 4 0.010 None 1.000 1 2019 2019
CUI: C0399572
Disease: Hypoplasia of mandibular condyle
Hypoplasia of mandibular condyle
phenotype Musculoskeletal Diseases; Stomatognathic Diseases Finding 4 2 0.100 None 0
Abnormality of the temporomandibular joint
phenotype Anatomical Abnormality 4 0.100 None 0
Aplasia/Hypoplasia of the external ear
phenotype Finding 4 0.100 None 0
CUI: C0268849
Disease: Overactive Detrusor
Overactive Detrusor
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 5 0.300 None 1.000 1 2004 2004
CUI: C0857094
Disease: Endometriosis related pain
Endometriosis related pain
disease Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C2243080
Disease: Intestinal necrosis
Intestinal necrosis
disease Digestive System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2003 2003
CUI: C4022171
Disease: Periauricular skin pits
Periauricular skin pits
disease Congenital Abnormality 5 1 0.100 None 0