IL4R, interleukin 4 receptor, 3566

N. diseases: 242; N. variants: 36
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: C4749142
Disease: MASTOCYTOSIS, INDOLENT
MASTOCYTOSIS, INDOLENT 		disease Disease or Syndrome 1 1 0.010 None 1.000 1 1 2001 2001
CUI: C1840084
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO 		disease Finding 1 1 0.100 None 0 1
CUI: C1840254
Disease: ATOPY, SUSCEPTIBILITY TO (finding)
ATOPY, SUSCEPTIBILITY TO (finding) 		phenotype Finding 1 1 0.100 None 0 1
CUI: C1853829
Disease: Arthropathy, Erosive
Arthropathy, Erosive 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 2012 2012
CUI: C1322281
Disease: Seasonal rhinitis
Seasonal rhinitis 		disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2009 2009
CUI: C0861154
Disease: Allergic rhinoconjunctivitis
Allergic rhinoconjunctivitis 		disease Eye Diseases; Immune System Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 2010 2010
CUI: C1276072
Disease: Adult atopic dermatitis
Adult atopic dermatitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 5 4 0.010 None 1.000 1 4 2000 2000
CUI: C1840253
Disease: IgE RESPONSIVENESS, ATOPIC
IgE RESPONSIVENESS, ATOPIC 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 5 0.300 None 0
CUI: C0585213
Disease: Minor oral aphthous ulceration
Minor oral aphthous ulceration 		disease Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0878631
Disease: pathergy
pathergy 		disease Disease or Syndrome 6 1 0.010 None 1.000 1 2011 2011
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Sign or Symptom 6 2 0.010 None 1.000 1 1 2006 2006
CUI: C1960047
Disease: Moderate persistent asthma
Moderate persistent asthma 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2001 2001
CUI: C0334419
Disease: Pheochromocytoma, malignant
Pheochromocytoma, malignant 		disease Neoplasms; Endocrine System Diseases Neoplastic Process 11 1 0.010 None 1.000 1 2009 2009
CUI: C0020523
Disease: Immediate hypersensitivity
Immediate hypersensitivity 		phenotype Immune System Diseases Pathologic Function 14 0.200 None 1.000 1 2010 2010
CUI: C0038363
Disease: Aphthous Stomatitis
Aphthous Stomatitis 		disease Stomatognathic Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2018 2018
CUI: C0276340
Disease: Respiratory syncytial virus bronchiolitis
Respiratory syncytial virus bronchiolitis 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 17 1 0.010 None 1.000 1 2003 2003
CUI: C0854706
Disease: Neonatal infection
Neonatal infection 		disease Disease or Syndrome 17 0.010 None 1.000 1 2017 2017
CUI: C1839735
Disease: MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME
MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 21 2 0.010 None 1.000 1 2012 2012
CUI: C0035450
Disease: Rheumatoid Nodule
Rheumatoid Nodule 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Acquired Abnormality 26 3 0.010 None 1.000 1 3 2010 2010
CUI: C0036221
Disease: Mast-Cell Sarcoma
Mast-Cell Sarcoma 		disease Neoplasms Neoplastic Process 27 4 0.010 None 1.000 1 2012 2012
CUI: C0036330
Disease: Schistosomiasis mansoni
Schistosomiasis mansoni 		disease Infections Disease or Syndrome 27 0.010 None < 0.001 1 2019 2019
CUI: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases; Nervous System Diseases; Endocrine System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 28 7 0.010 None 1.000 1 1 2012 2012
CUI: C0155880
Disease: Intrinsic asthma
Intrinsic asthma 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 29 5 0.010 None 1.000 1 1 2001 2001
CUI: C0947961
Disease: Atopic disorders
Atopic disorders 		group Disease or Syndrome 29 2 0.010 None 1.000 1 1 1999 1999
CUI: C0027583
Disease: Nematode infections
Nematode infections 		group Infections Disease or Syndrome 33 0.020 None 1.000 2 2017 2018