HP, haptoglobin, 3240

N. diseases: 464; N. variants: 9
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: C0016479
Disease: Food Poisoning
Food Poisoning
disease Chemically-Induced Disorders Injury or Poisoning 1 0.300 None 1.000 1 2011 2011
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
disease Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2016 2016
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease
group Chemically-Induced Disorders Injury or Poisoning 1 0.300 None 1.000 1 2011 2011
CUI: C0341934
Disease: Transient hypertension of pregnancy
Transient hypertension of pregnancy
phenotype Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases Pathologic Function 2 0.300 None 1.000 1 2006 2006
CUI: C4025182
Disease: Exercise-induced hemolysis
Exercise-induced hemolysis
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C3279786
Disease: ANHAPTOGLOBINEMIA
ANHAPTOGLOBINEMIA
disease Disease or Syndrome 3 1 0.420 None 1.000 3 1 2004 2015
CUI: C0036474
Disease: Scurvy
Scurvy
disease Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 3 0.010 None 1.000 1 2007 2007
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections
group Infections Disease or Syndrome 3 0.300 None 1.000 1 2006 2006
CUI: C0221152
Disease: Obstipation
Obstipation
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017
CUI: C0234972
Disease: Convulsive disorder
Convulsive disorder
disease Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2004 2004
CUI: C0268419
Disease: Acatalasia
Acatalasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 1 0.010 None 1.000 1 2003 2003
CUI: C2931868
Disease: Catalase deficiency
Catalase deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2003 2003
Hereditary fructose intolerance syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 47 0.010 None 1.000 1 2017 2017
CUI: C0019054
Disease: Hemolysis (disorder)
Hemolysis (disorder)
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 1 2014 2014
CUI: C0280257
Disease: stage, esophageal cancer
stage, esophageal cancer
disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2019 2019
CUI: C0312854
Disease: Extravascular Hemolysis
Extravascular Hemolysis
disease Pathological Conditions, Signs and Symptoms Pathologic Function 6 0.300 None 1.000 1 2014 2014
Malignant neoplasm of upper lobe, bronchus or lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 7 0.200 None 1.000 1 2009 2009
Malignant neoplasm of middle lobe, bronchus or lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 7 0.200 None 1.000 1 2009 2009
Malignant neoplasm of lower lobe, bronchus or lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 7 0.200 None 1.000 1 2009 2009
Malignant neoplasm of other parts of bronchus or lung
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 7 0.200 None 1.000 1 2009 2009
CUI: C0341047
Disease: Hypertrophy of parotid gland
Hypertrophy of parotid gland
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Stomatognathic Diseases Disease or Syndrome 7 0.010 None 1.000 1 1976 1976
CUI: C0741975
Disease: carotid disease
carotid disease
disease Disease or Syndrome 7 5 0.010 None < 0.001 1 2011 2011
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 8 2 0.010 None 1.000 1 1993 1993
CUI: C0857862
Disease: Staphylococcus Aureus Pneumonia
Staphylococcus Aureus Pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 8 0.010 None 1.000 1 2019 2019
Irritable bowel syndrome characterized by constipation
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2019 2019