GRK2, G protein-coupled receptor kinase 2, 156

N. diseases: 159; 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: C0520540
Disease: Rebound hypertension
Rebound hypertension 		disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1997092
Disease: Hypertensive left ventricular hypertrophy
Hypertensive left ventricular hypertrophy 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2004 2004
CUI: C0012684
Disease: Blastocyst Disintegration
Blastocyst Disintegration 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 7 0.300 None 1.000 1 2006 2006
CUI: C0013937
Disease: Embryo Resorption
Embryo Resorption 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Organism Function 7 0.300 None 1.000 1 2006 2006
CUI: C0752350
Disease: Embryo Death
Embryo Death 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 7 0.300 None 1.000 1 2006 2006
CUI: C1136082
Disease: Embryo Disintegration
Embryo Disintegration 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 7 0.300 None 1.000 1 2006 2006
CUI: C0679309
Disease: physical symptom
physical symptom 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2019 2019
CUI: C0752351
Disease: Embryo Loss
Embryo Loss 		phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Pathologic Function 11 0.300 None 1.000 1 2006 2006
CUI: C0496870
Disease: Benign neoplasm of liver
Benign neoplasm of liver 		disease Digestive System Diseases; Neoplasms Neoplastic Process 13 0.010 None 1.000 1 2019 2019
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 15 0.010 None 1.000 1 2018 2018
CUI: C1273070
Disease: Left ventricular diastolic dysfunction
Left ventricular diastolic dysfunction 		disease Cardiovascular Diseases Disease or Syndrome 31 1 0.010 None 1.000 1 2020 2020
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
Takotsubo Cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 44 3 0.010 None 1.000 1 2018 2018
CUI: C0158570
Disease: Vascular anomaly
Vascular anomaly 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 47 5 0.010 None 1.000 1 2013 2013
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
Sessile Serrated Adenoma/Polyp 		disease Neoplastic Process 48 6 0.010 None 1.000 1 2013 2013
CUI: C1135191
Disease: Heart Failure, Systolic
Heart Failure, Systolic 		disease Cardiovascular Diseases Disease or Syndrome 49 6 0.010 None 1.000 1 2019 2019
CUI: C0392164
Disease: Pulmonary Cystic Fibrosis
Pulmonary Cystic Fibrosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 53 0.010 None 1.000 1 2002 2002
CUI: C1849157
Disease: Resistance to Insulin-Like Growth Factor I
Resistance to Insulin-Like Growth Factor I 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 55 4 0.020 None 1.000 2 2016 2017
CUI: C0393642
Disease: Sepsis-Associated Encephalopathy
Sepsis-Associated Encephalopathy 		disease Nervous System Diseases Disease or Syndrome 57 0.010 None 1.000 1 2018 2018
CUI: C0040411
Disease: Tongue Neoplasms
Tongue Neoplasms 		group Neoplasms; Stomatognathic Diseases Neoplastic Process 62 0.010 None 1.000 1 2019 2019
CUI: C2004489
Disease: Regurgitation
Regurgitation 		phenotype Sign or Symptom 66 0.010 None 1.000 1 2019 2019
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 72 4 0.010 None 1.000 1 2018 2018
CUI: C0239849
Disease: Harlequin Fetus
Harlequin Fetus 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 73 1 0.010 None 1.000 1 2014 2014
CUI: C2118460
Disease: Acute colitis
Acute colitis 		disease Digestive System Diseases Disease or Syndrome 83 0.010 None 1.000 1 2018 2018
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism 		disease Endocrine System Diseases Disease or Syndrome 84 6 0.020 None 1.000 2 2016 2019
CUI: C1383860
Disease: Cardiac Hypertrophy
Cardiac Hypertrophy 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 88 11 0.300 None 1.000 1 2002 2002