KLRD1, killer cell lectin like receptor D1, 3824

N. diseases: 53; N. variants: 2
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.
adult nasal type extranodal NK/T-cell lymphoma
disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2003 2003
childhood nasal type extranodal NK/T-cell lymphoma
disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2003 2003
Chronic Lymphoproliferative Disorder of NK-Cells
disease Pathological Conditions, Signs and Symptoms Neoplastic Process 17 0.010 None 1.000 1 2018 2018
CUI: C0033839
Disease: Pseudorabies
Pseudorabies
disease Infections; Nervous System Diseases; Animal Diseases Disease or Syndrome 49 0.010 None 1.000 1 2019 2019
Nasal Type Extranodal NK/T-Cell Lymphoma
disease Neoplasms Neoplastic Process 53 0.010 None 1.000 1 2003 2003
CUI: C0021345
Disease: Infectious Mononucleosis
Infectious Mononucleosis
disease Infections; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 58 4 0.010 None < 0.001 1 2007 2007
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis
disease Infections; Nervous System Diseases Disease or Syndrome 88 4 0.010 None 1.000 1 2003 2003
CUI: C0008055
Disease: Chikungunya Fever
Chikungunya Fever
disease Infections Disease or Syndrome 137 10 0.010 None 1.000 1 2017 2017
High-Grade Squamous Intraepithelial Lesions
phenotype Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 150 8 0.010 None 1.000 1 2013 2013
CUI: C0019562
Disease: Von Hippel-Lindau Syndrome
Von Hippel-Lindau Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 174 187 0.010 None 1.000 1 1992 1992
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
disease Neoplasms Neoplastic Process 179 34 0.010 None < 0.001 1 2007 2007
CUI: C0035435
Disease: Rheumatism
Rheumatism
disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 197 19 0.010 None 1.000 1 2003 2003
CUI: C0276447
Disease: Rhinovirus infection
Rhinovirus infection
disease Infections Disease or Syndrome 202 4 0.010 None 1.000 1 2018 2018
CUI: C0867389
Disease: Chronic graft-versus-host disease
Chronic graft-versus-host disease
disease Immune System Diseases Disease or Syndrome 241 17 0.010 None 1.000 1 2016 2016
CUI: C2745900
Disease: Promyelocytic leukemia
Promyelocytic leukemia
disease Neoplastic Process 255 2 0.010 None 1.000 1 2017 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 2001 2001
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura
disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 338 35 0.010 None 1.000 1 2017 2017
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic
disease Digestive System Diseases; Infections Disease or Syndrome 415 84 0.010 None 1.000 1 2010 2010
CUI: C4552766
Disease: Miscarriage
Miscarriage
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 426 56 0.010 None 1.000 1 2005 2005
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
disease Infections Disease or Syndrome 429 42 0.010 None 1.000 1 2013 2013
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
disease Digestive System Diseases; Infections Disease or Syndrome 430 80 0.020 None 1.000 2 2004 2018
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
disease Immune System Diseases Disease or Syndrome 447 25 0.010 None 1.000 1 2003 2003
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections
group Infections Disease or Syndrome 462 26 0.080 None 1.000 8 2004 2019
CUI: C3714514
Disease: Infection
Infection
group Infections Pathologic Function 491 0.010 None 1.000 1 2004 2004
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases Disease or Syndrome 502 243 0.010 None < 0.001 1 2007 2007