CAT, catalase, 847

N. diseases: 794; N. variants: 14
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: C0752048
Disease: Hypocatalasemia
Hypocatalasemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.320 None 1.000 7 1990 2015
CUI: C2936847
Disease: Acatalasemia Japanese type
Acatalasemia Japanese type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.310 None 1.000 6 1990 2015
CUI: C2936848
Disease: Acatalasemia Swiss type
Acatalasemia Swiss type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.300 None 1.000 5 1990 2015
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
group Infections Disease or Syndrome 1 0.010 None 1.000 1 2009 2009
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas
disease Congenital Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0333295
Disease: Acute ulcer
Acute ulcer
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 1 0.010 None 1.000 1 2011 2011
CUI: C0523550
Disease: Catalase measurement
Catalase measurement
phenotype Laboratory Procedure 1 2 0.100 None 1.000 1 1 2017 2017
CUI: C0746604
Disease: Mitral valve endocarditis
Mitral valve endocarditis
disease Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
CUI: C1171363
Disease: Renoprival hypertension
Renoprival hypertension
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.200 None 1.000 1 2012 2012
CUI: C1536651
Disease: Arterial leg ulcer
Arterial leg ulcer
disease Disease or Syndrome 1 0.010 None 1.000 1 2008 2008
CUI: C1963823
Disease: Hyperlipasaemia
Hyperlipasaemia
disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C2363972
Disease: Histaminosis
Histaminosis
disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4022869
Disease: Reduced catalase activity
Reduced catalase activity
phenotype Finding 1 0.100 None 0
CUI: C0241266
Disease: Subcutaneous Abscess
Subcutaneous Abscess
disease Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C0242453
Disease: Prostatism
Prostatism
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 1 0.010 None 1.000 1 2016 2016
CUI: C0271407
Disease: Synchysis scintillans
Synchysis scintillans
disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0342873
Disease: Glutaric Aciduria III
Glutaric Aciduria III
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 2 0.010 None 1.000 1 2019 2019
CUI: C1263758
Disease: Female genital tract infection
Female genital tract infection
group Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 2 0.010 None 1.000 1 2007 2007
CUI: C4039867
Disease: Acute hypoxemic respiratory failure
Acute hypoxemic respiratory failure
disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0268419
Disease: Acatalasia
Acatalasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 1 0.700 strong 1.000 19 1 1988 2019
CUI: C2931868
Disease: Catalase deficiency
Catalase deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.540 None 1.000 9 1990 2015
CUI: C0003177
Disease: Cutaneous anthrax
Cutaneous anthrax
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0276651
Disease: Aspergilloma
Aspergilloma
disease Infections; Respiratory Tract Diseases Disease or Syndrome 3 0.010 None 1.000 1 2006 2006
CUI: C0282526
Disease: Hyperpipecolic Acidemia
Hyperpipecolic Acidemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C1740794
Disease: Aortic wall hypertrophy
Aortic wall hypertrophy
disease Disease or Syndrome 3 0.010 None 1.000 1 2005 2005