NFKB1, nuclear factor kappa B subunit 1, 4790

N. diseases: 551; N. variants: 52
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: C4225277
Disease: IMMUNODEFICIENCY, COMMON VARIABLE, 12
IMMUNODEFICIENCY, COMMON VARIABLE, 12 		disease Disease or Syndrome 1 6 0.400 strong 1.000 3 6 2015 2018
CUI: C0085164
Disease: Leukemia, Feline
Leukemia, Feline 		disease Neoplasms; Infections; Animal Diseases Neoplastic Process 3 0.010 None 1.000 1 2006 2006
CUI: C1275192
Disease: Subungual keratoacanthoma
Subungual keratoacanthoma 		disease Skin and Connective Tissue Diseases Neoplastic Process 3 0.010 None 1.000 1 2011 2011
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: C1298681
Disease: Oxalosis
Oxalosis 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 9 0.300 None 1.000 1 2005 2005
CUI: C1337012
Disease: Well-differentiated papillary mesothelioma
Well-differentiated papillary mesothelioma 		disease Neoplasms Neoplastic Process 9 0.010 None 1.000 1 2019 2019
CUI: C2981712
Disease: Ocular Adnexal Lymphoma
Ocular Adnexal Lymphoma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 9 0.010 None 1.000 1 2013 2013
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: C2936665
Disease: Immunoglobulin Deficiency, Late-Onset
Immunoglobulin Deficiency, Late-Onset 		disease Immune System Diseases Disease or Syndrome 11 0.300 None 0
CUI: C0340782
Disease: Hyperplastic lymph node
Hyperplastic lymph node 		disease Acquired Abnormality 12 0.010 None < 0.001 1 1991 1991
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft 		phenotype Finding 12 0.100 None 0
CUI: C1318518
Disease: Infantile malignant osteopetrosis
Infantile malignant osteopetrosis 		disease Musculoskeletal Diseases Congenital Abnormality 13 0.010 None 1.000 1 2019 2019
CUI: C0206675
Disease: Adenomatoid Tumor
Adenomatoid Tumor 		disease Neoplasms Neoplastic Process 14 0.010 None 1.000 1 2019 2019
CUI: C0020192
Disease: Hyaline Membrane Disease
Hyaline Membrane Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases Disease or Syndrome 15 0.010 None 1.000 1 2005 2005
CUI: C0085923
Disease: soft neurological signs
soft neurological signs 		phenotype Sign or Symptom 15 1 0.010 None 1.000 1 2007 2007
CUI: C3494358
Disease: Prodromal Symptoms
Prodromal Symptoms 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 15 4 0.010 None 1.000 1 2004 2004
CUI: C0006274
Disease: Bronchiolitis, Viral
Bronchiolitis, Viral 		disease Infections; Respiratory Tract Diseases Disease or Syndrome 16 0.010 None 1.000 1 2016 2016
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections 		phenotype Finding 16 0.400 strong 1.000 1 2015 2015
CUI: C0152264
Disease: Familial erythrocytosis
Familial erythrocytosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 17 2 0.010 None 1.000 1 2007 2007
CUI: C0270496
Disease: Schizoaffective disorder, bipolar type
Schizoaffective disorder, bipolar type 		disease Mental Disorders Mental or Behavioral Dysfunction 17 10 0.010 None 1.000 1 2007 2007
CUI: C0333355
Disease: Inflammatory disease of mucous membrane
Inflammatory disease of mucous membrane 		group Digestive System Diseases; Stomatognathic Diseases Pathologic Function 18 0.010 None 1.000 1 2007 2007
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 18 18 0.010 None 1.000 1 2001 2001