HP, haptoglobin, 3240

N. diseases: 411; N. variants: 8
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: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic Diseases Disease or Syndrome 41 13 0.010 None 1.000 1 2018 2018
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: C0267026
Disease: Actinic cheilitis
Actinic cheilitis
disease Stomatognathic Diseases Disease or Syndrome 64 8 0.010 None 1.000 1 1992 1992
CUI: C0600433
Disease: Activated Protein C Resistance
Activated Protein C Resistance
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 40 23 0.010 None 1.000 1 2002 2002
Acute exacerbation of chronic obstructive airways disease
phenotype Respiratory Tract Diseases Disease or Syndrome 63 1 0.010 None 1.000 1 2018 2018
Acute Inflammatory Demyelinating Polyneuropathy
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2018 2018
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
Acute Motor Axonal Neuropathy
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 14 4 0.010 None 1.000 1 2018 2018
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 765 118 0.070 None 1.000 7 1989 2019
CUI: C2882221
Disease: Acute pulmonary embolism
Acute pulmonary embolism
disease Respiratory Tract Diseases; Cardiovascular Diseases Disease or Syndrome 42 0.010 None 1.000 1 2018 2018
CUI: C0748355
Disease: Acute respiratory distress
Acute respiratory distress
disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 147 6 0.010 None 1.000 1 2019 2019
CUI: C0234935
Disease: Acute urticaria
Acute urticaria
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 17 0.010 None 1.000 1 2018 2018
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
group Neoplasms Neoplastic Process 2080 167 0.010 None 1.000 1 2009 2009
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
disease Neoplasms Neoplastic Process 2246 183 0.010 None 1.000 1 2018 2018
CUI: C1569637
Disease: Adenocarcinoma, Endometrioid
Adenocarcinoma, Endometrioid
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases Neoplastic Process 129 4 0.010 None 1.000 1 2010 2010
CUI: C0001430
Disease: Adenoma
Adenoma
group Neoplasms Neoplastic Process 1126 103 0.010 None 1.000 1 2020 2020
CUI: C1609524
Disease: ADHF
ADHF
disease Disease or Syndrome 46 0.010 None 1.000 1 2019 2019
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
disease Neoplasms Neoplastic Process 2527 98 0.020 None 1.000 2 2001 2010
CUI: C4543811
Disease: Adult-onset immunodeficiency
Adult-onset immunodeficiency
disease Immune System Diseases Disease or Syndrome 9 1 0.010 None 1.000 1 2017 2017
CUI: C0041228
Disease: African Trypanosomiasis
African Trypanosomiasis
disease Infections Disease or Syndrome 54 2 0.010 None 1.000 1 2017 2017
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
disease Eye Diseases Disease or Syndrome 616 390 0.020 None 1.000 1 2003 2018
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 471 223 0.010 None 1.000 1 1979 1979
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 85 16 0.030 None 1.000 3 2006 2014
CUI: C1456873
Disease: alpha^+^ Thalassemia
alpha^+^ Thalassemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 92 13 0.030 None 1.000 3 2006 2014
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3131 968 0.070 None 0.857 7 1984 2020
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 685 93 0.040 None 0.750 4 1985 2019