IL1RN, interleukin 1 receptor antagonist, 3557

N. diseases: 701; N. variants: 52
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: C0341461
Disease: Idiopathic acute pancreatitis
Idiopathic acute pancreatitis 		disease Disease or Syndrome 1 0.010 None 1.000 1 2000 2000
CUI: C1532322
Disease: Infectious Endophthalmitis
Infectious Endophthalmitis 		disease Infections; Eye Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C2675112
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 (finding) 		disease Finding 1 0.500 None 0
CUI: C0376699
Disease: Teeth, Endodontically-Treated
Teeth, Endodontically-Treated 		disease Stomatognathic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2013 2013
CUI: C2748507
Disease: INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 3 2 0.740 strong 1.000 6 2 2009 2017
CUI: C0796081
Disease: Myhre syndrome
Myhre syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 3 7 0.010 None 1.000 1 2013 2013
CUI: C0152087
Disease: Crystal Arthropathies
Crystal Arthropathies 		group Musculoskeletal Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C1168305
Disease: Corneal melt
Corneal melt 		disease Disease or Syndrome 4 0.010 None 1.000 1 2000 2000
CUI: C2826320
Disease: Refractory Neutropenia
Refractory Neutropenia 		disease Hemic and Lymphatic Diseases Neoplastic Process 4 1 0.010 None 1.000 1 2012 2012
CUI: C4749462
Disease: New-onset refractory status epilepticus
New-onset refractory status epilepticus 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0153257
Disease: Primary pulmonary coccidioidomycosis
Primary pulmonary coccidioidomycosis 		disease Pathological Conditions, Signs and Symptoms; Infections; Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0158353
Disease: Infectious Myositis
Infectious Myositis 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 5 0.300 None 1.000 1 2000 2000
CUI: C0403528
Disease: Henoch-Schönlein nephritis
Henoch-Schönlein nephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 5 0.010 None 1.000 1 1997 1997
CUI: C0544796
Disease: Myositis, Proliferative
Myositis, Proliferative 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 5 0.300 None 1.000 1 2000 2000
CUI: C0751357
Disease: Myositis, Focal
Myositis, Focal 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 5 0.300 None 1.000 1 2000 2000
CUI: C0015378
Disease: Extravasation of Contrast Media
Extravasation of Contrast Media 		phenotype Pathological Conditions, Signs and Symptoms; Wounds and Injuries Pathologic Function 6 0.300 None 1.000 1 1995 1995
CUI: C0235842
Disease: Decidual endometritis
Decidual endometritis 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 6 0.010 None 1.000 1 2008 2008
CUI: C0856737
Disease: Single vessel disease
Single vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 6 0.010 None 1.000 1 2001 2001
CUI: C3826476
Disease: Dental caries in children
Dental caries in children 		disease Disease or Syndrome 6 0.010 None 1.000 1 2019 2019
CUI: C0031111
Disease: Periostitis
Periostitis 		disease Infections; Musculoskeletal Diseases Disease or Syndrome 6 0.100 None 0
CUI: C0267561
Disease: Perianal fistula
Perianal fistula 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases Anatomical Abnormality 7 2 0.010 None 1.000 1 2001 2001
CUI: C0741975
Disease: carotid disease
carotid disease 		disease Disease or Syndrome 7 5 0.010 None 1.000 1 2 2010 2010
CUI: C4049262
Disease: Febrile infection related epilepsy syndrome
Febrile infection related epilepsy syndrome 		disease Nervous System Diseases Disease or Syndrome 8 2 0.020 None 1.000 2 2016 2019
CUI: C1290638
Disease: Resorption of apex of tooth root
Resorption of apex of tooth root 		disease Stomatognathic Diseases Disease or Syndrome 8 0.010 None 1.000 1 2012 2012
CUI: C0242993
Disease: Nephropathia Epidemica
Nephropathia Epidemica 		disease Infections Disease or Syndrome 9 0.020 None 1.000 2 2001 2008