CHRM3, cholinergic receptor muscarinic 3, 1131

N. diseases: 122; N. variants: 7
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: C0033770
Disease: Prune Belly Syndrome
Prune Belly Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 19 2 0.620 1.000 3 1 2005 2018
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Congenital Abnormality 413 15 0.400 1 2012 2012
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 13 0.310 1.000 1 2012 2012
CUI: C1262760
Disease: Hepatitis, Drug-Induced
Hepatitis, Drug-Induced
disease Digestive System Diseases; Substance-Related Disorders Disease or Syndrome 328 0.300 1 2010 2010
CUI: C4279912
Disease: Chemically-Induced Liver Toxicity
Chemically-Induced Liver Toxicity
disease Digestive System Diseases; Substance-Related Disorders Disease or Syndrome 324 0.300 1 2010 2010
CUI: C0019193
Disease: Hepatitis, Toxic
Hepatitis, Toxic
disease Digestive System Diseases; Substance-Related Disorders Injury or Poisoning 324 0.300 1 2010 2010
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
disease Digestive System Diseases Disease or Syndrome 682 71 0.300 1 2010 2010
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Congenital Abnormality 9 0.300 1 2012 2012
CUI: C1563731
Disease: Inguinal Cryptorchidism
Inguinal Cryptorchidism
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Finding 9 0.300 1 2012 2012
CUI: C0431663
Disease: Bilateral Cryptorchidism
Bilateral Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Congenital Abnormality 20 4 0.300 1 2012 2012
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease
disease Digestive System Diseases; Substance-Related Disorders Disease or Syndrome 376 45 0.300 1 2010 2010
CUI: C0431664
Disease: Unilateral Cryptorchidism
Unilateral Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases; Male Urogenital Diseases Congenital Abnormality 13 1 0.300 1 2012 2012
CUI: C3658290
Disease: Drug-Induced Acute Liver Injury
Drug-Induced Acute Liver Injury
disease Digestive System Diseases; Substance-Related Disorders Disease or Syndrome 324 0.300 1 2010 2010
Chemical and Drug Induced Liver Injury
disease Digestive System Diseases; Substance-Related Disorders Disease or Syndrome 324 0.300 1 2010 2010
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
disease Digestive System Diseases Disease or Syndrome 544 31 0.300 1 2010 2010
CUI: C0003962
Disease: Ascites
Ascites
phenotype Pathological Conditions, Signs and Symptoms Finding 44 0.300 1 2010 2010
CUI: C1968949
Disease: Cakut
Cakut
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 70 3 0.300 limited 0
CUI: C0265363
Disease: Urethral obstruction sequence
Urethral obstruction sequence
disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 1 0.300 0
Megacystis microcolon intestinal hypoperistalsis syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome 5 12 0.200 1 2000 2000
CUI: C0014544
Disease: Epilepsy
Epilepsy
disease Nervous System Diseases Disease or Syndrome 1176 147 0.110 1.000 2 1 2012 2013
CUI: C0009806
Disease: Constipation
Constipation
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 207 7 0.110 1.000 1 2016 2016
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
phenotype Laboratory Procedure 25 50 0.100 1 1 2018 2018
Soluble Interleukin 6 Receptor Measurement
phenotype Laboratory Procedure 32 297 0.100 1 1 2018 2018
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
phenotype Organ or Tissue Function 100 929 0.100 1 1 2016 2016
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
phenotype Cardiovascular Diseases Disease or Syndrome 83 186 0.100 1 1 2013 2013