TACR1, tachykinin receptor 1, 6869

N. diseases: 217; N. variants: 10
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: C0406299
Disease: Chronic prurigo
Chronic prurigo
disease Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0006261
Disease: Bronchial Diseases
Bronchial Diseases
group Respiratory Tract Diseases Disease or Syndrome 6 0.300 None 1.000 1 2005 2005
CUI: C0149523
Disease: Acute cystitis
Acute cystitis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C2074900
Disease: Chronic postoperative pain
Chronic postoperative pain
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 7 0.010 None 1.000 1 2017 2017
CUI: C2945767
Disease: Childhood Malignant Liver Neoplasm
Childhood Malignant Liver Neoplasm
disease Digestive System Diseases; Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2015 2015
CUI: C0752235
Disease: Lyme Neuroborreliosis
Lyme Neuroborreliosis
disease Infections; Nervous System Diseases Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C0263353
Disease: Prurigo nodularis
Prurigo nodularis
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 12 0.010 None 1.000 1 2019 2019
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis
disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 13 0.200 None 1.000 1 2000 2000
CUI: C0600467
Disease: Neurogenic Inflammation
Neurogenic Inflammation
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Injury or Poisoning 18 0.500 None 1.000 3 2007 2011
CUI: C0850758
Disease: Pelvic pain female
Pelvic pain female
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 20 0.010 None 1.000 1 2019 2019
CUI: C3160917
Disease: Bladder pain syndrome
Bladder pain syndrome
disease Disease or Syndrome 20 0.010 None 1.000 1 2019 2019
CUI: C1321905
Disease: Minimal Brain Dysfunction
Minimal Brain Dysfunction
disease Mental Disorders Mental or Behavioral Dysfunction 22 0.300 None 1.000 1 2010 2010
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
phenotype Behavior and Behavior Mechanisms Sign or Symptom 23 10 0.010 None 1.000 1 2019 2019
CUI: C0030794
Disease: Pelvic Pain
Pelvic Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 23 0.010 None 1.000 1 2019 2019
CUI: C0349217
Disease: Depressive episode, unspecified
Depressive episode, unspecified
disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 27 2 0.010 None < 0.001 1 2019 2019
CUI: C1568363
Disease: Tendinosis
Tendinosis
disease Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 28 0.010 None < 0.001 1 2008 2008
CUI: C0520909
Disease: Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 31 18 0.010 None 1.000 1 1 2015 2015
CUI: C0877430
Disease: Asthma chronic
Asthma chronic
disease Disease or Syndrome 36 0.010 None 1.000 1 2018 2018
CUI: C0231749
Disease: Knee pain
Knee pain
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Sign or Symptom 38 6 0.010 None 1.000 1 2017 2017
CUI: C0178782
Disease: Orofacial Pain
Orofacial Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 40 0.010 None 1.000 1 2017 2017
CUI: C2919828
Disease: Chronic ulcerative colitis
Chronic ulcerative colitis
disease Digestive System Diseases Disease or Syndrome 40 0.010 None 1.000 1 2011 2011
CUI: C0391976
Disease: Pain Disorder
Pain Disorder
disease Mental Disorders Mental or Behavioral Dysfunction 41 3 0.010 None 1.000 1 2001 2001
CUI: C1961121
Disease: Congenital vascular anomaly
Congenital vascular anomaly
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 42 1 0.010 None 1.000 1 2017 2017
Fenestration (morphologic abnormality)
disease Acquired Abnormality 43 0.010 None 1.000 1 2019 2019
CUI: C0007684
Disease: Central Nervous System Infection
Central Nervous System Infection
group Infections; Nervous System Diseases Disease or Syndrome 44 5 0.010 None 1.000 1 2017 2017