A2M, alpha-2-macroglobulin, 2

N. diseases: 147; N. variants: 3
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: C3279661
Disease: alpha-2-Macroglobulin Deficiency
alpha-2-Macroglobulin Deficiency 		disease Respiratory Tract Diseases Disease or Syndrome 1 0.310 None 1.000 1 1989 1989
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		phenotype Finding 2 3 0.100 None 0 1
CUI: C0473119
Disease: Fecal peritonitis
Fecal peritonitis 		disease Digestive System Diseases; Infections Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C0238096
Disease: Embolism, Paradoxical
Embolism, Paradoxical 		disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2007 2007
CUI: C4703620
Disease: Decreased level of GABA in serum
Decreased level of GABA in serum 		phenotype Finding 6 0.100 None 0
CUI: C0015814
Disease: Femur Head Necrosis
Femur Head Necrosis 		disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 8 0.200 None 1.000 1 2010 2010
CUI: C0015951
Disease: Fetal Resorption
Fetal Resorption 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 8 0.010 None 1.000 1 2014 2014
CUI: C0029823
Disease: Other specified peritonitis
Other specified peritonitis 		disease Digestive System Diseases; Infections Disease or Syndrome 8 0.200 None 1.000 1 2006 2006
CUI: C1865903
Disease: Long-tract signs
Long-tract signs 		phenotype Finding 9 0.100 None 0
CUI: C0375381
Disease: Urethral intrinsic sphincter deficiency
Urethral intrinsic sphincter deficiency 		disease Disease or Syndrome 14 0.010 None 1.000 1 2019 2019
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		disease Disease or Syndrome 18 7 0.010 None 1.000 1 1 2002 2002
CUI: C0085400
Disease: Neurofibrillary degeneration (morphologic abnormality)
Neurofibrillary degeneration (morphologic abnormality) 		phenotype Cell or Molecular Dysfunction 21 0.100 None 0
CUI: C0041227
Disease: Trypanosomiasis
Trypanosomiasis 		disease Infections Disease or Syndrome 23 0.200 None 1.000 1 2007 2007
CUI: C0014059
Disease: Encephalomyelitis, Acute Disseminated
Encephalomyelitis, Acute Disseminated 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 24 0.010 None 1.000 1 2019 2019
CUI: C1527352
Disease: Hepatic Form of Wilson Disease
Hepatic Form of Wilson Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24 0.300 None 1.000 1 2013 2013
CUI: C0040038
Disease: Thromboembolism
Thromboembolism 		phenotype Cardiovascular Diseases Pathologic Function 25 3 0.010 None 1.000 1 2007 2007
CUI: C0027019
Disease: Myelomonocytic leukemia
Myelomonocytic leukemia 		disease Neoplasms Neoplastic Process 36 0.010 None 1.000 1 1995 1995
CUI: C0019243
Disease: Angioedemas, Hereditary
Angioedemas, Hereditary 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 54 7 0.010 None 1.000 1 1996 1996
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 57 17 0.010 None 1.000 1 2016 2016
CUI: C0600327
Disease: Toxic Shock Syndrome
Toxic Shock Syndrome 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 61 0.200 None 1.000 1 1986 1986
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		disease Nutritional and Metabolic Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 65 22 0.010 None 1.000 1 1999 1999
CUI: C0221757
Disease: alpha 1-Antitrypsin Deficiency
alpha 1-Antitrypsin Deficiency 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 73 48 0.020 None 0.500 2 1981 1983
CUI: C0694549
Disease: Community acquired pneumonia
Community acquired pneumonia 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 75 13 0.010 None 1.000 1 2018 2018
CUI: C0042025
Disease: Urinary Stress Incontinence
Urinary Stress Incontinence 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 79 5 0.010 None 1.000 1 2019 2019
CUI: C1720830
Disease: Painful Bladder Syndrome
Painful Bladder Syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 81 0.010 None 1.000 1 2017 2017