CD40, CD40 molecule, 958

N. diseases: 528; N. variants: 21
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: C1334069
Disease: Hyperimmunoglobulin Syndrome
Hyperimmunoglobulin Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 1 0.010 None 1.000 1 2015 2015
CUI: C2721575
Disease: Ischemic nephropathy
Ischemic nephropathy 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C1720957
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 3
Hyper-IgM Immunodeficiency Syndrome, Type 3 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 3 0.700 None 1.000 3 3 2001 2016
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 0.020 None 1.000 2 2005 2016
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
CUI: C2348037
Disease: CD40 Ligand Deficiency
CD40 Ligand Deficiency 		disease Immune System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2003 2003
CUI: C1720956
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 2
Hyper-IgM Immunodeficiency Syndrome, Type 2 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 14 0.300 None 0
CUI: C1720958
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 5
Hyper-IgM Immunodeficiency Syndrome, Type 5 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 3 2 0.300 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: C1842528
Disease: Impaired Ig class switch recombination
Impaired Ig class switch recombination 		phenotype Finding 4 0.100 None 0
CUI: C1847383
Disease: Absence of lymph node germinal center
Absence of lymph node germinal center 		phenotype Finding 4 0.100 None 0
CUI: C0233746
Disease: Perceptual disturbance
Perceptual disturbance 		disease Mental Disorders Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2007 2007
CUI: C0021151
Disease: Incipient Schizophrenia
Incipient Schizophrenia 		disease Mental Disorders Mental or Behavioral Dysfunction 6 0.010 None 1.000 1 2007 2007
CUI: C0730315
Disease: Acute central serous chorioretinopathy
Acute central serous chorioretinopathy 		disease Infections; Eye Diseases Disease or Syndrome 7 3 0.010 None 1.000 1 2019 2019
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 0.010 None 1.000 1 1993 1993
CUI: C1847973
Disease: Persistent Polyclonal B-Cell Lymphocytosis
Persistent Polyclonal B-Cell Lymphocytosis 		disease Hemic and Lymphatic Diseases Disease or Syndrome 8 0.010 None 1.000 1 2001 2001
CUI: C1399819
Disease: Humoral immunodeficiency
Humoral immunodeficiency 		disease Immune System Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2010 2010
CUI: C0032870
Disease: Poxviridae Infections
Poxviridae Infections 		group Infections Disease or Syndrome 10 0.010 None 1.000 1 1997 1997
CUI: C0240805
Disease: Prodrome
Prodrome 		phenotype Sign or Symptom 10 0.010 None 1.000 1 2004 2004
CUI: C1846006
Disease: Ectodermal dysplasia, hypohidrotic, with immune deficiency
Ectodermal dysplasia, hypohidrotic, with immune deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 10 13 0.010 None 1.000 1 2008 2008
CUI: C0016204
Disease: Flatulence
Flatulence 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 11 0.010 None 1.000 1 2012 2012
CUI: C4330050
Disease: WHO Grade II Glioma
WHO Grade II Glioma 		disease Neoplastic Process 11 0.010 None 1.000 1 2019 2019
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 0.400 None 1.000 12 1994 2019
CUI: C0810032
Disease: Pancreatic disorders (not diabetes)
Pancreatic disorders (not diabetes) 		group Digestive System Diseases Disease or Syndrome 13 6 0.010 None 1.000 1 2008 2008