CHRM3, cholinergic receptor muscarinic 3, 1131

N. diseases: 284; N. variants: 17
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: C0265363
Disease: Urethral obstruction sequence
Urethral obstruction sequence
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 1 2011 2011
Aplasia of the abdominal wall musculature
phenotype Finding 1 0.100 None 0
CUI: C0266335
Disease: Congenital anomaly of the bladder
Congenital anomaly of the bladder
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 3 0.010 None 1.000 1 2011 2011
CUI: C2363280
Disease: Cervical auricle (disorder)
Cervical auricle (disorder)
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases Congenital Abnormality 4 0.010 None 1.000 1 2013 2013
CUI: C0021479
Disease: INJECTED EYE
INJECTED EYE
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Sign or Symptom 6 0.010 None 1.000 1 2018 2018
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 8 0.300 None 1.000 1 2011 2011
CUI: C1563731
Disease: Inguinal Cryptorchidism
Inguinal Cryptorchidism
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Finding 8 0.300 None 1.000 1 2011 2011
Megacystis microcolon intestinal hypoperistalsis syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome 9 3 0.200 None 1.000 1 2000 2000
CUI: C0158458
Disease: Acquired hallux valgus
Acquired hallux valgus
disease Musculoskeletal Diseases Acquired Abnormality 14 0.010 None 1.000 1 2020 2020
CUI: C0265656
Disease: Congenital hallux valgus
Congenital hallux valgus
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 14 0.010 None 1.000 1 2020 2020
CUI: C0858762
Disease: Neuro-Behcet disease
Neuro-Behcet disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 17 15 0.010 None 1.000 1 2018 2018
CUI: C0431664
Disease: Unilateral Cryptorchidism
Unilateral Cryptorchidism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases Congenital Abnormality 17 5 0.300 None 1.000 1 2011 2011
Soluble Interleukin 6 Receptor Measurement
phenotype Laboratory Procedure 17 25 0.100 None 1.000 1 1 2017 2017
CUI: C0221760
Disease: brain cyst
brain cyst
disease Disease or Syndrome 18 0.060 None 1.000 6 2011 2019
CUI: C4021972
Disease: Urogenital sinus anomaly
Urogenital sinus anomaly
disease Anatomical Abnormality 18 0.100 None 0
CUI: C0021828
Disease: Intestinal Atresia
Intestinal Atresia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome 20 2 0.100 None 0
CUI: C0043154
Disease: Dental White Spot
Dental White Spot
disease Stomatognathic Diseases Disease or Syndrome 22 0.010 None 1.000 1 2019 2019
Nonarteritic anterior ischemic optic neuropathy (NAION)
disease Disease or Syndrome 22 6 0.010 None 1.000 1 2018 2018
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 24 0.320 None 1.000 2 2011 2019
CUI: C0026961
Disease: Mydriasis
Mydriasis
phenotype Eye Diseases Sign or Symptom 25 2 0.010 None 1.000 1 2019 2019
Congenital posterior urethral valves
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 26 1 0.100 None 0
CUI: C0740766
Disease: Acute pneumonia
Acute pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 29 0.010 None 1.000 1 2019 2019
CUI: C4024996
Disease: Aplasia/Hypoplasia of the lungs
Aplasia/Hypoplasia of the lungs
phenotype Finding 29 0.100 None 0
CUI: C0520909
Disease: Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 31 18 0.020 None 1.000 2 1 2014 2018