NCF1, neutrophil cytosolic factor 1, 653361

N. diseases: 170; N. variants: 11
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.
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 593 24 0.010 None 1.000 1 2013 2013
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.010 None 1.000 1 2011 2011
CUI: C2242826
Disease: Myeloblastic leukemia
Myeloblastic leukemia
disease Neoplastic Process 22 0.010 None 1.000 1 2002 2002
Acute disseminated encephalitis and encephalomyelitis (ADEM)
disease Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III
disease Disease or Syndrome 3 2 0.100 None 1.000 1 1 2015 2015
Selective immunoglobulin A deficiency
disease Disease or Syndrome 45 23 0.010 None 1.000 1 2008 2008
CUI: C4049446
Disease: Neointimal hyperplasia
Neointimal hyperplasia
disease Disease or Syndrome 198 0.010 None 1.000 1 2017 2017
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
disease Disease or Syndrome 741 81 0.010 None 1.000 1 2019 2019
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality
phenotype Finding 74 1 0.100 None 0
CUI: C0521173
Disease: Granulomatosis
Granulomatosis
disease Disease or Syndrome 14 1 0.100 None 0
CUI: C1835686
Disease: Recurrent bacterial skin infections
Recurrent bacterial skin infections
phenotype Finding 13 1 0.100 None 0
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule
phenotype Finding 59 2 0.100 None 0
Absence of bactericidal oxidative respiratory burst in phagocytes
phenotype Finding 4 0.100 None 0
CUI: C1844394
Disease: Decreased activity of NADPH oxidase
Decreased activity of NADPH oxidase
phenotype Finding 5 0.100 None 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
phenotype Finding 175 0.100 None 0
Recurrent Staphylococcus aureus infections
phenotype Finding 11 1 0.100 None 0
CUI: C4020969
Disease: Inflammatory abnormality of the eye
Inflammatory abnormality of the eye
disease Disease or Syndrome 88 1 0.100 None 0
CUI: C4021751
Disease: Recurrent Klebsiella infections
Recurrent Klebsiella infections
phenotype Finding 5 0.100 None 0
CUI: C4021752
Disease: Recurrent Aspergillus infections
Recurrent Aspergillus infections
phenotype Finding 5 0.100 None 0
Recurrent Burkholderia cepacia infections
phenotype Finding 4 0.100 None 0
Recurrent Serratia marcescens infections
phenotype Finding 4 0.100 None 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.350 None 1.000 8 2006 2013
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.020 None 1.000 2 2009 2015
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
disease Cardiovascular Diseases Disease or Syndrome 2044 281 0.020 None 1.000 2 2009 2015
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal
disease Cardiovascular Diseases Disease or Syndrome 586 90 0.310 None 1.000 2 2006 2017