BGN, biglycan, 633

N. diseases: 253; 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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		phenotype Neoplastic Process 6626 169 0.090 None 1.000 9 2007 2019
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		disease Disease or Syndrome 593 24 0.030 None 1.000 3 2016 2018
CUI: C1402315
Disease: Vascular lesions
Vascular lesions 		disease Disease or Syndrome 111 9 0.020 None 1.000 2 2004 2017
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		disease Acquired Abnormality 115 15 0.020 None 1.000 2 2007 2010
CUI: C4707243
Disease: Familial thoracic aortic aneurysm and aortic dissection
Familial thoracic aortic aneurysm and aortic dissection 		disease Disease or Syndrome 59 442 0.500 limited 1.000 2 2007 2017
CUI: C0028259
Disease: Nodule
Nodule 		phenotype Acquired Abnormality 278 19 0.010 None 1.000 1 2016 2016
CUI: C0238421
Disease: Selenium deficiency
Selenium deficiency 		disease Disease or Syndrome 44 0.010 None 1.000 1 2019 2019
CUI: C0272138
Disease: Erythroblastosis
Erythroblastosis 		disease Disease or Syndrome 89 0.010 None 1.000 1 2013 2013
CUI: C0334037
Disease: Intestinal metaplasia
Intestinal metaplasia 		phenotype Disease or Syndrome 266 24 0.010 None 1.000 1 2019 2019
CUI: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow 		disease Acquired Abnormality 73 14 0.010 None 1.000 1 2005 2005
CUI: C0426359
Disease: Urinary symptoms
Urinary symptoms 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2019 2019
CUI: C0694571
Disease: extranodal lymphoma
extranodal lymphoma 		disease Neoplastic Process 17 1 0.010 None 1.000 1 2018 2018
CUI: C1833142
Disease: contracture of elbow
contracture of elbow 		phenotype Acquired Abnormality 2 0.010 None 1.000 1 2005 2005
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis 		phenotype Disease or Syndrome 328 0.010 None 1.000 1 2000 2000
CUI: C2827469
Disease: Coronary Microvascular Disease
Coronary Microvascular Disease 		disease Disease or Syndrome 45 3 0.010 None 1.000 1 2008 2008
CUI: C2945695
Disease: Limb ischemia
Limb ischemia 		disease Disease or Syndrome 171 3 0.010 None 1.000 1 2009 2009
CUI: C3840085
Disease: Disorder of Achilles tendon
Disorder of Achilles tendon 		disease Disease or Syndrome 33 28 0.010 None 1.000 1 2006 2006
CUI: C3888569
Disease: Degenerative aortic valve disease
Degenerative aortic valve disease 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C4020848
Disease: Aneurysmal disease
Aneurysmal disease 		disease Disease or Syndrome 14 0.010 None 1.000 1 1998 1998
CUI: C4310811
Disease: MEESTER-LOEYS SYNDROME
MEESTER-LOEYS SYNDROME 		disease Disease or Syndrome 1 3 0.700 strong 1.000 1 3 2017 2017
CUI: C4324549
Disease: Perimyocarditis
Perimyocarditis 		disease Disease or Syndrome 5 0.010 None 1.000 1 2011 2011
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		disease Neoplastic Process 3669 502 0.010 None 1.000 1 2012 2012
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla 		disease Congenital Abnormality 113 5 0.100 None 0
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		phenotype Finding 391 49 0.100 None 0
CUI: C0426807
Disease: Short clavicle
Short clavicle 		phenotype Finding 26 0.100 None 0