MT2A, metallothionein 2A, 4502

N. diseases: 117; 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: C0334268
Disease: Schneiderian papilloma
Schneiderian papilloma
disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 2015 2015
CUI: C0154742
Disease: Other lesions of median nerve
Other lesions of median nerve
phenotype Nervous System Diseases Pathologic Function 8 0.200 None 1.000 1 2012 2012
3 beta-Hydroxysteroid dehydrogenase deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 9 25 0.010 None 1.000 1 2002 2002
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 13 8 0.010 None 1.000 1 2000 2000
CUI: C0268060
Disease: Juvenile hemochromatosis
Juvenile hemochromatosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 18 8 0.010 None 1.000 1 2015 2015
CUI: C0001349
Disease: Acute-Phase Reaction
Acute-Phase Reaction
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 24 0.200 None 1.000 1 1999 1999
T-cell/histiocyte rich large B-cell lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 28 0.010 None 1.000 1 2013 2013
CUI: C0349218
Disease: Recurrent depressive disorder
Recurrent depressive disorder
disease Mental Disorders Mental or Behavioral Dysfunction 29 9 0.310 None 1.000 1 2011 2011
CUI: C0746556
Disease: metabolic disturbance
metabolic disturbance
disease Disease or Syndrome 29 4 0.010 None 1.000 1 2015 2015
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 32 21 0.200 None 1.000 1 2010 2010
CUI: C1695782
Disease: Cerebral hypoperfusion
Cerebral hypoperfusion
disease Disease or Syndrome 40 1 0.010 None 1.000 1 2017 2017
CUI: C1881254
Disease: Inverted Squamous Cell Papilloma
Inverted Squamous Cell Papilloma
disease Neoplasms Neoplastic Process 46 1 0.010 None 1.000 1 1 2015 2015
CUI: C0206721
Disease: Inverted Papilloma
Inverted Papilloma
disease Neoplasms Neoplastic Process 51 1 0.010 None 1.000 1 1 2015 2015
CUI: C0403447
Disease: Chronic Kidney Insufficiency
Chronic Kidney Insufficiency
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 52 12 0.300 None 1.000 1 2016 2016
CUI: C0018023
Disease: Nodular Goiter
Nodular Goiter
disease Endocrine System Diseases Disease or Syndrome 55 12 0.010 None 1.000 1 2017 2017
Multiple Endocrine Neoplasia Type 2a
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases Neoplastic Process 69 44 0.010 None 1.000 1 1986 1986
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 85 11 0.010 None 1.000 1 2000 2000
CUI: C1383860
Disease: Cardiac Hypertrophy
Cardiac Hypertrophy
phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 88 11 0.300 None 1.000 1 2001 2001
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency
disease Nutritional and Metabolic Diseases Disease or Syndrome 90 4 0.010 None 1.000 1 2005 2005
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 98 9 0.010 None 1.000 1 2007 2007
CUI: C2937421
Disease: Prostatic Hyperplasia
Prostatic Hyperplasia
disease Male Urogenital Diseases Disease or Syndrome 112 1 0.010 None 1.000 1 2008 2008
CUI: C0016034
Disease: Breast Fibrocystic Disease
Breast Fibrocystic Disease
disease Skin and Connective Tissue Diseases Disease or Syndrome 114 12 0.010 None 1.000 1 2015 2015
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 122 78 0.200 None 1.000 1 2006 2006
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid
disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 123 10 0.010 None 1.000 1 2006 2006
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 135 19 0.010 None 1.000 1 2007 2007