CD40LG, CD40 ligand, 959

N. diseases: 453; N. variants: 25
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: C0852689
Disease: Congenital rubella infection
Congenital rubella infection
disease Disease or Syndrome; Congenital Abnormality 1 0.010 None 1.000 1 2014 2014
Indirect Contact Transmission Infection
phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0276687
Disease: Disseminated cryptococcosis
Disseminated cryptococcosis
disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C1882620
Disease: Rat Cholangiofibrosis
Rat Cholangiofibrosis
disease Disease or Syndrome 2 0.200 None 1.000 1 2013 2013
CUI: C1863767
Disease: Light Fixation Seizure Syndrome
Light Fixation Seizure Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 3 0.040 None 1.000 4 1993 2016
CUI: C0035921
Disease: Congenital Rubella Syndrome
Congenital Rubella Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections Disease or Syndrome 3 0.010 None 1.000 1 2000 2000
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 3 1 0.200 None 1.000 1 2006 2006
HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 8 0.010 None 1.000 1 2001 2001
CUI: C0549123
Disease: Large tonsils (finding)
Large tonsils (finding)
phenotype Pathological Conditions, Signs and Symptoms Finding 3 0.100 None 0
CUI: C4025672
Disease: Impaired memory B cell generation
Impaired memory B cell generation
phenotype Cell or Molecular Dysfunction 3 0.100 None 0
CUI: C0241932
Disease: X-linked hypogammaglobulinemia
X-linked hypogammaglobulinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 4 0.010 None 1.000 1 1996 1996
Impaired Ig class switch recombination
phenotype Finding 4 0.100 None 0
Absence of lymph node germinal center
phenotype Finding 4 0.100 None 0
CUI: C0262534
Disease: White Coat Hypertension
White Coat Hypertension
disease Cardiovascular Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C1608955
Disease: Mycobacterium abscessus Infection
Mycobacterium abscessus Infection
disease Infections Disease or Syndrome 6 0.010 None 1.000 1 2015 2015
CUI: C1846550
Disease: Decreased T cell activation
Decreased T cell activation
phenotype Finding 6 0.100 None 0
CUI: C4049279
Disease: Post stroke epilepsy
Post stroke epilepsy
disease Disease or Syndrome 7 2 0.010 None 1.000 1 2014 2014
CUI: C0745242
Disease: Immunoglobulin deficiency
Immunoglobulin deficiency
disease Immune System Diseases Disease or Syndrome 8 0.020 None 1.000 2 1993 2018
CUI: C0024303
Disease: Small Cell Lymphoma
Small Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 1975 1975
CUI: C0853602
Disease: Immunodeficiency congenital
Immunodeficiency congenital
disease Disease or Syndrome; Congenital Abnormality 8 0.010 None 1.000 1 2001 2001
CUI: C2609059
Disease: Antisynthetase syndrome
Antisynthetase syndrome
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2020 2020
CUI: C0013374
Disease: Dysgammaglobulinemia
Dysgammaglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 10 0.110 None 1.000 1 2000 2000
CUI: C3203657
Disease: Autoimmune retinopathy
Autoimmune retinopathy
disease Eye Diseases; Immune System Diseases Disease or Syndrome 10 0.010 None 1.000 1 2005 2005
CUI: C0272236
Disease: Hyperimmunoglobulin M syndrome
Hyperimmunoglobulin M syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 12 1 0.200 strong 1.000 32 1 1993 2018
CUI: C0005866
Disease: Bluetongue infection
Bluetongue infection
disease Infections; Animal Diseases Disease or Syndrome 13 0.010 None 1.000 1 2019 2019