F2RL1, F2R like trypsin receptor 1, 2150

N. diseases: 256; N. variants: 4
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: C0036502
Disease: Sebaceous Gland Diseases
Sebaceous Gland Diseases 		group Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C0856687
Disease: Infection caused by Trichinella
Infection caused by Trichinella 		disease Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C1333034
Disease: Chronic Cancer Pain
Chronic Cancer Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 4 1 0.010 None 1.000 1 2012 2012
CUI: C0347073
Disease: Carcinoma in situ of mouth
Carcinoma in situ of mouth 		disease Neoplasms; Stomatognathic Diseases Neoplastic Process 6 0.010 None 1.000 1 2013 2013
CUI: C0001420
Disease: Papillary adenocarcinoma
Papillary adenocarcinoma 		disease Neoplasms Neoplastic Process 11 3 0.010 None 1.000 1 2004 2004
CUI: C0948249
Disease: Femoral artery occlusion
Femoral artery occlusion 		disease Cardiovascular Diseases Disease or Syndrome 12 0.010 None 1.000 1 2017 2017
CUI: C0153453
Disease: Malignant tumor of extrahepatic bile duct
Malignant tumor of extrahepatic bile duct 		disease Digestive System Diseases; Neoplasms Neoplastic Process 14 0.010 None 1.000 1 2011 2011
CUI: C0730321
Disease: Punctate inner choroidopathy
Punctate inner choroidopathy 		disease Eye Diseases Disease or Syndrome 14 0.010 None 1.000 1 2019 2019
CUI: C0747479
Disease: Periodontal infection
Periodontal infection 		disease Disease or Syndrome 17 0.020 None 1.000 2 2013 2017
CUI: C0948908
Disease: Nephrotoxic serum nephritis
Nephrotoxic serum nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2019 2019
CUI: C0018188
Disease: Granuloma
Granuloma 		phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Pathologic Function 24 0.010 None 1.000 1 2006 2006
CUI: C0031094
Disease: Periodontal Pocket
Periodontal Pocket 		disease Stomatognathic Diseases Anatomical Abnormality 28 0.010 None 1.000 1 2017 2017
CUI: C0151785
Disease: Disease of mucous membrane
Disease of mucous membrane 		group Pathological Conditions, Signs and Symptoms Disease or Syndrome 30 0.010 None 1.000 1 2019 2019
CUI: C0234252
Disease: Mechanical pain
Mechanical pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 30 4 0.010 None 1.000 1 2018 2018
CUI: C0345964
Disease: Adenoma of lung
Adenoma of lung 		disease Neoplasms Neoplastic Process 30 3 0.010 None 1.000 1 2005 2005
CUI: C4744444
Disease: Metastatic Lung Adenocarcinoma
Metastatic Lung Adenocarcinoma 		disease Neoplasms Neoplastic Process 34 10 0.010 None 1.000 1 2019 2019
CUI: C0238019
Disease: Carcinoma of extrahepatic bile duct
Carcinoma of extrahepatic bile duct 		disease Digestive System Diseases; Neoplasms Neoplastic Process 35 0.010 None 1.000 1 2011 2011
CUI: C0876991
Disease: Histiocytosis haematophagic
Histiocytosis haematophagic 		disease Disease or Syndrome 36 2 0.020 None 1.000 2 2013 2015
CUI: C0948780
Disease: Rhinosinusitis
Rhinosinusitis 		disease Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 38 1 0.010 None 1.000 1 2007 2007
CUI: C0022577
Disease: Keratoconjunctivitis, Vernal
Keratoconjunctivitis, Vernal 		disease Eye Diseases; Immune System Diseases Disease or Syndrome 40 0.010 None 1.000 1 2005 2005
CUI: C1855038
Disease: Hepatocellular necrosis
Hepatocellular necrosis 		phenotype Disease or Syndrome 41 0.010 None 1.000 1 2016 2016
CUI: C1536148
Disease: Chocolate cyst of ovary
Chocolate cyst of ovary 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 50 4 0.010 None 1.000 1 2011 2011
CUI: C1262048
Disease: Glial scar
Glial scar 		phenotype Acquired Abnormality 51 0.010 None 1.000 1 2019 2019
CUI: C1262211
Disease: Diarrhoea predominant irritable bowel syndrome
Diarrhoea predominant irritable bowel syndrome 		disease Disease or Syndrome 57 8 0.020 None 1.000 2 2010 2015
CUI: C0234245
Disease: Visceral Pain
Visceral Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 58 0.010 None 1.000 1 2019 2019