BRD4, bromodomain containing 4, 23476

N. diseases: 335; N. variants: 6
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: C2675993
Disease: Pancreatic squamous cell carcinoma
Pancreatic squamous cell carcinoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 3 0.100 None 0
CUI: C1802395
Disease: Congenital muscular hypertrophy-cerebral syndrome
Congenital muscular hypertrophy-cerebral syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 50 0.300 None 1.000 1 2018 2018
CUI: C1853099
Disease: Cornelia de Lange Syndrome 3
Cornelia de Lange Syndrome 3 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 5 20 0.300 None 1.000 1 2018 2018
CUI: C0334489
Disease: Pancreatoblastoma
Pancreatoblastoma 		disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 6 0.100 None 0
CUI: C4551851
Disease: Cornelia de Lange Syndrome 1
Cornelia de Lange Syndrome 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 8 266 0.300 None 1.000 1 2018 2018
CUI: C0887850
Disease: Polycystic Kidney, Type 1 Autosomal Dominant Disease
Polycystic Kidney, Type 1 Autosomal Dominant Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 10 2 0.300 None 1.000 1 2015 2015
CUI: C0949570
Disease: Wheat Hypersensitivity
Wheat Hypersensitivity 		disease Immune System Diseases Disease or Syndrome 11 2 0.010 None 1.000 1 2009 2009
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum 		phenotype Anatomical Abnormality 12 0.100 None 0
CUI: C0263477
Disease: Female pattern alopecia (disorder)
Female pattern alopecia (disorder) 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 15 0.300 None 1.000 1 2014 2014
CUI: C1142536
Disease: Pneumonia due to methicillin resistant Staphylococcus aureus
Pneumonia due to methicillin resistant Staphylococcus aureus 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 15 0.010 None 1.000 1 2015 2015
CUI: C2751306
Disease: Polycystic kidney disease, type 2
Polycystic kidney disease, type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 15 41 0.300 None 1.000 1 2015 2015
CUI: C0740919
Disease: Allergy to grass pollen
Allergy to grass pollen 		disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 17 0.010 None 1.000 1 2011 2011
CUI: C1865285
Disease: Megalencephaly cutis marmorata telangiectatica congenita
Megalencephaly cutis marmorata telangiectatica congenita 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 18 18 0.010 None 1.000 1 2018 2018
CUI: C1868594
Disease: Perry Syndrome
Perry Syndrome 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 19 9 0.020 None 1.000 2 2009 2010
CUI: C1443237
Disease: Healthcare associated pneumonia
Healthcare associated pneumonia 		phenotype Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 22 2 0.010 None 1.000 1 2017 2017
CUI: C3890429
Disease: Liquid Tumor
Liquid Tumor 		disease Neoplastic Process 22 0.010 None 1.000 1 2019 2019
CUI: C0086873
Disease: Pseudopelade
Pseudopelade 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 23 0.300 None 1.000 1 2014 2014
CUI: C4285066
Disease: Double-Hit Lymphoma
Double-Hit Lymphoma 		disease Neoplastic Process 24 0.010 None 1.000 1 2019 2019
CUI: C3280586
Disease: Mannose-Binding Protein Deficiency
Mannose-Binding Protein Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 25 3 0.010 None < 0.001 1 2013 2013
CUI: C0312414
Disease: Menstrual spotting
Menstrual spotting 		phenotype Sign or Symptom 27 2 0.010 None 1.000 1 2017 2017
CUI: C4727069
Disease: Advanced Renal Cell Carcinoma
Advanced Renal Cell Carcinoma 		disease Neoplastic Process 27 0.010 None 1.000 1 2018 2018
CUI: C1827301
Disease: Extensively Drug-Resistant Tuberculosis
Extensively Drug-Resistant Tuberculosis 		phenotype Infections Disease or Syndrome 29 0.010 None 1.000 1 2016 2016
CUI: C3669246
Disease: Mammary adenocarcinoma
Mammary adenocarcinoma 		disease Neoplastic Process 29 0.010 None 1.000 1 2004 2004
CUI: C0007125
Disease: Carcinoma, Ehrlich Tumor
Carcinoma, Ehrlich Tumor 		disease Neoplasms Neoplastic Process; Experimental Model of Disease 30 0.010 None 1.000 1 2018 2018
CUI: C0014009
Disease: Empyema
Empyema 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 31 0.010 None 1.000 1 2013 2013