CNTN2, contactin 2, 6900

N. diseases: 99; N. variants: 14
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: C1608408
Disease: Malignant transformation
Malignant transformation
phenotype Neoplastic Process 1027 20 0.030 None 1.000 3 2001 2009
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 2 3 2018 2018
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
phenotype Laboratory Procedure 717 1599 0.100 None 1.000 1 1 2016 2016
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
phenotype Organism Attribute 565 1138 0.100 None 1.000 1 1 2019 2019
Central nervous system demyelination
disease Disease or Syndrome 52 3 0.010 None 1.000 1 2018 2018
Human T-cell lymphotrophic virus, type I [HTLV-I]
disease Disease or Syndrome 25 0.010 None 1.000 1 2012 2012
CUI: C0596887
Disease: mathematical ability
mathematical ability
phenotype Mental Process 854 2127 0.100 None 1.000 1 3 2018 2018
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.010 None 1.000 1 1994 1994
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.010 None 1.000 1 1997 1997
Corpuscular Hemoglobin Concentration Mean
phenotype Laboratory or Test Result 401 4389 0.100 None 1.000 1 3 2012 2012
CUI: C0239842
Disease: Tremor of hands
Tremor of hands
phenotype Sign or Symptom 31 7 0.100 None 0
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5
disease Disease or Syndrome 1 1 0.600 None 0 1
CUI: C0024054
Disease: Lown-Ganong-Levine Syndrome
Lown-Ganong-Levine Syndrome
disease Cardiovascular Diseases Disease or Syndrome 9 0.010 None 1.000 1 2009 2009
CUI: C0025958
Disease: Microcephaly
Microcephaly
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Congenital Abnormality 1064 27 0.010 None 1.000 1 2001 2001
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 311 827 0.010 None 1.000 1 1996 1996
CUI: C0162678
Disease: Neurofibromatoses
Neurofibromatoses
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 135 16 0.010 None 1.000 1 1996 1996
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 481 47 0.030 None 1.000 3 1993 2000
CUI: C0005956
Disease: Bone Marrow Diseases
Bone Marrow Diseases
group Hemic and Lymphatic Diseases Disease or Syndrome 84 3 0.010 None 1.000 1 1996 1996
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
group Immune System Diseases Disease or Syndrome 1758 428 0.020 None 1.000 2 1999 2017
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
group Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 300 14 0.010 None 1.000 1 1996 1996
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 82 4 0.030 None 1.000 3 1 2009 2012
CUI: C0393847
Disease: Multifocal motor neuropathy
Multifocal motor neuropathy
disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 13 0.010 None < 0.001 1 2011 2011
CUI: C0020097
Disease: HTLV-I Infections
HTLV-I Infections
group Infections; Immune System Diseases Disease or Syndrome 134 5 0.050 None 1.000 5 1990 2013
CUI: C0242338
Disease: HTLV Infections
HTLV Infections
group Infections; Immune System Diseases Disease or Syndrome 8 0.010 None 1.000 1 2012 2012
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis
disease Infections; Nervous System Diseases Disease or Syndrome 88 4 0.080 None 1.000 8 1993 2010