NOTCH4, notch receptor 4, 4855

N. diseases: 150; N. variants: 58
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: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 3 0.010 None 1.000 1 1 2017 2017
CUI: C0457533
Disease: Desmoplastic ameloblastoma
Desmoplastic ameloblastoma
disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2010 2010
Intracranial Arteriovenous Malformation
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Congenital Abnormality 11 0.200 None 0
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
phenotype Laboratory Procedure 12 15 0.100 None 1.000 1 1 2012 2012
CUI: C1656427
Disease: Early onset schizophrenia
Early onset schizophrenia
disease Mental or Behavioral Dysfunction 15 3 0.020 None 0.500 2 2006 2006
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 15 3 0.010 None 1.000 1 2019 2019
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
phenotype Laboratory Procedure 15 16 0.100 None 1.000 1 1 2013 2013
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
phenotype Laboratory Procedure 17 25 0.100 None 1.000 1 1 2017 2017
CUI: C3544321
Disease: Treatment-resistant schizophrenia
Treatment-resistant schizophrenia
disease Mental or Behavioral Dysfunction 23 2 0.310 None 1.000 1 1 2015 2015
CUI: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 37 7 0.100 None 1.000 1 1 2014 2014
CUI: C0231921
Disease: Pulmonary function
Pulmonary function
phenotype Organ or Tissue Function 41 259 0.100 None 1.000 1 1 2010 2010
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding)
phenotype Finding 41 259 0.100 None 1.000 1 1 2010 2010
CUI: C0078911
Disease: AIDS-Associated Nephropathy
AIDS-Associated Nephropathy
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 45 1 0.210 None 1.000 2 2010 2019
CUI: C0043037
Disease: Common wart
Common wart
disease Neoplasms; Infections; Skin and Connective Tissue Diseases Disease or Syndrome 48 0.010 None 1.000 1 2005 2005
CUI: C0206706
Disease: Verrucous carcinoma
Verrucous carcinoma
disease Neoplasms Neoplastic Process 49 0.010 None 1.000 1 2019 2019
CUI: C0543697
Disease: Mixed cryoglobulinemia
Mixed cryoglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 56 5 0.010 None 1.000 1 1 2017 2017
Aspartate aminotransferase measurement
phenotype Laboratory Procedure 57 76 0.100 None 1.000 1 1 2018 2018
CUI: C0562350
Disease: Hip circumference
Hip circumference
phenotype Clinical Attribute 68 116 0.100 None 1.000 1 1 2019 2019
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases Neoplastic Process 76 14 0.010 None 1.000 1 2017 2017
CUI: C0280785
Disease: Diffuse Astrocytoma
Diffuse Astrocytoma
disease Neoplasms Neoplastic Process 81 8 0.010 None 1.000 1 2014 2014
CUI: C0887833
Disease: Carcinoma, Pancreatic Ductal
Carcinoma, Pancreatic Ductal
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 82 0.300 None 1.000 1 2009 2009
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
Inclusion Body Myopathy, Sporadic
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 84 5 0.010 None 1.000 1 2012 2012
Pancreatic Intraductal Papillary Mucinous Neoplasm
disease Digestive System Diseases; Neoplasms; Endocrine System Diseases Neoplastic Process 84 8 0.010 None 1.000 1 2016 2016
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula
phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Anatomical Abnormality 93 8 0.010 None 1.000 1 2017 2017
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
disease Stomatognathic Diseases Disease or Syndrome 104 101 0.100 None 1.000 1 1 2019 2019