B2M, beta-2-microglobulin, 567

N. diseases: 352; N. variants: 6
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: C0472386
Disease: Progressive post hemorrhagic ventricular dilatation
Progressive post hemorrhagic ventricular dilatation 		disease Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C4054590
Disease: Lupus Flare
Lupus Flare 		disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C4302669
Disease: Autosomal dominant beta2-microglobulinic amyloidosis
Autosomal dominant beta2-microglobulinic amyloidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.300 None 1.000 1 2012 2012
CUI: C1855796
Disease: Hypoproteinemia, Hypercatabolic
Hypoproteinemia, Hypercatabolic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 2 0.710 strong 1.000 2 2 2006 2015
CUI: C0013533
Disease: Echovirus Infections
Echovirus Infections 		group Infections Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C1536074
Disease: Osteoarticular pain
Osteoarticular pain 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2017 2017
CUI: C0268405
Disease: Hemodialysis-associated amyloidosis
Hemodialysis-associated amyloidosis 		disease Nutritional and Metabolic Diseases Disease or Syndrome 3 0.050 None 1.000 5 1994 2019
CUI: C0267988
Disease: Hyperproteinemia
Hyperproteinemia 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4509023
Disease: Light chain (AL) amyloidosis
Light chain (AL) amyloidosis 		disease Disease or Syndrome 3 0.010 None 1.000 1 1996 1996
CUI: C4021578
Disease: Chronic axonal neuropathy
Chronic axonal neuropathy 		disease Disease or Syndrome 5 0.100 None 0
CUI: C4025212
Disease: Autonomic bladder dysfunction
Autonomic bladder dysfunction 		disease Nervous System Diseases Disease or Syndrome 5 1 0.100 None 0
CUI: C0865440
Disease: (non-specific) purulent meningitis
(non-specific) purulent meningitis 		disease Disease or Syndrome 6 0.010 None < 0.001 1 2018 2018
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition 		phenotype Nutritional and Metabolic Diseases Finding 6 0.100 None 0
CUI: C1843273
Disease: Tubulointerstitial nephritis and uveitis
Tubulointerstitial nephritis and uveitis 		disease Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases Disease or Syndrome 7 3 0.010 None 1.000 1 2017 2017
CUI: C3489398
Disease: Neuroepithelioma, Peripheral
Neuroepithelioma, Peripheral 		disease Neoplasms; Skin and Connective Tissue Diseases; Nervous System Diseases Neoplastic Process 7 0.010 None 1.000 1 1993 1993
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 8 15 0.700 None 1.000 1 1 2012 2012
CUI: C0272362
Disease: Acquired von Willebrand's disease
Acquired von Willebrand's disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 8 1 0.010 None 1.000 1 2020 2020
CUI: C1858266
Disease: Bare Lymphocyte Syndrome, Type I
Bare Lymphocyte Syndrome, Type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 8 3 0.300 None 1.000 1 2015 2015
CUI: C1608393
Disease: Megacystis microcolon intestinal hypoperistalsis syndrome
Megacystis microcolon intestinal hypoperistalsis syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 2018 2018
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 6 0.040 None 1.000 4 1 2012 2017
CUI: C1519787
Disease: Undifferentiated Neuroblastoma
Undifferentiated Neuroblastoma 		disease Neoplasms Neoplastic Process 12 0.010 None 1.000 1 1993 1993
CUI: C0856738
Disease: Triple vessel disease
Triple vessel disease 		disease Cardiovascular Diseases Disease or Syndrome 13 3 0.010 None 1.000 1 2019 2019
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 14 9 0.010 None 1.000 1 2011 2011
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 14 9 0.010 None 1.000 1 2013 2013
CUI: C0085663
Disease: Plasmacytosis
Plasmacytosis 		disease Pathological Conditions, Signs and Symptoms; Neoplasms Disease or Syndrome 15 0.030 None 0.667 3 1995 2006