HMOX1, heme oxygenase 1, 3162

N. diseases: 510; N. variants: 6
Source: BEFREE ×
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: C0276876
Disease: Infection by Leishmania infantum
Infection by Leishmania infantum
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2012 2012
CUI: C0391860
Disease: Diffuse inflammation
Diffuse inflammation
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1 0.010 None 1.000 1 2016 2016
CUI: C0518959
Disease: Left atrial myxoma
Left atrial myxoma
disease Neoplastic Process 1 0.010 None 1.000 1 2014 2014
CUI: C2350449
Disease: Pancreatitis, Graft
Pancreatitis, Graft
disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2007 2007
CUI: C4706275
Disease: Sickle cell hepatopathy
Sickle cell hepatopathy
disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2011 2011
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
disease Cardiovascular Diseases Disease or Syndrome 4 1 0.010 None 1.000 1 2019 2019
CUI: C0497249
Disease: hypertension complicated
hypertension complicated
disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C4531013
Disease: Light induced retinopathy
Light induced retinopathy
disease Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0347073
Disease: Carcinoma in situ of mouth
Carcinoma in situ of mouth
disease Neoplasms; Stomatognathic Diseases Neoplastic Process 6 0.010 None 1.000 1 2013 2013
Proliferative diabetic retinopathy - quiescent
disease Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C1442981
Disease: Alcoholic liver damage
Alcoholic liver damage
disease Digestive System Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
Antley-Bixler Syndrome with Disordered Steroidogenesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 6 3 0.010 None 1.000 1 2010 2010
CUI: C0032870
Disease: Poxviridae Infections
Poxviridae Infections
group Infections Disease or Syndrome 10 0.010 None 1.000 1 2014 2014
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Hemic and Lymphatic Diseases Congenital Abnormality 10 3 0.010 None 1.000 1 2011 2011
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma
disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 2018 2018
CUI: C4476910
Disease: Thin-cap fibroatheroma
Thin-cap fibroatheroma
phenotype Cardiovascular Diseases Acquired Abnormality 12 0.010 None 1.000 1 2010 2010
CUI: C0086447
Disease: Ileal Pouches
Ileal Pouches
disease Acquired Abnormality 13 0.010 None 1.000 1 2001 2001
CUI: C0149875
Disease: Primary dysmenorrhea
Primary dysmenorrhea
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 13 3 0.010 None 1.000 1 2017 2017
CUI: C0152517
Disease: Viral gastroenteritis
Viral gastroenteritis
group Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Infections Disease or Syndrome 15 1 0.010 None 1.000 1 2017 2017
CUI: C0400877
Disease: Postoperative ileus
Postoperative ileus
disease Digestive System Diseases Disease or Syndrome 17 0.010 None 1.000 1 2020 2020
Carbamoyl-Phosphate Synthase I Deficiency Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 19 3 0.010 None 1.000 1 2010 2010
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease
disease Digestive System Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 20 0.010 None 1.000 1 2018 2018
CUI: C0037061
Disease: Siderosis
Siderosis
disease Respiratory Tract Diseases; Occupational Diseases Disease or Syndrome 20 2 0.010 None 1.000 1 2017 2017
CUI: C0162568
Disease: Erythropoietic Protoporphyria
Erythropoietic Protoporphyria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 21 3 0.010 None 1.000 1 2017 2017