NBN, nibrin, 4683

N. diseases: 291; N. variants: 194
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: C0155781
Disease: Thrombosed internal hemorrhoids
Thrombosed internal hemorrhoids
disease Digestive System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C3806428
Disease: Progressive vitiligo
Progressive vitiligo
phenotype Skin and Connective Tissue Diseases Finding 1 0.100 None 0
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
disease Finding 3 2277 0.100 None 0 1
CUI: C0024904
Disease: Mastoiditis
Mastoiditis
disease Infections; Musculoskeletal Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 5 0.100 None 0
CUI: C0220754
Disease: Biotinidase Deficiency
Biotinidase Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 6 187 0.010 None 1.000 1 2009 2009
CUI: C0042023
Disease: Increased frequency of micturition
Increased frequency of micturition
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 6 0.100 None 0
CUI: C0740372
Disease: Gastrointestinal lymphoma
Gastrointestinal lymphoma
disease Digestive System Diseases; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2006 2006
CUI: C0013374
Disease: Dysgammaglobulinemia
Dysgammaglobulinemia
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 10 0.100 None 0
CUI: C1858732
Disease: Malar prominence
Malar prominence
phenotype Finding 10 0.100 None 0
Ataxia-Telangiectasisa-Like Disorder 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 15 0.020 None 1.000 2 1 2008 2009
CUI: C1858391
Disease: ATAXIA-TELANGIECTASIA-LIKE DISORDER
ATAXIA-TELANGIECTASIA-LIKE DISORDER
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 12 13 0.020 None 1.000 2 1 2008 2009
CUI: C0178416
Disease: Hypoplastic anemia
Hypoplastic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 12 0.300 None 0
CUI: C1879362
Disease: Hypertyrosinemia
Hypertyrosinemia
disease Disease or Syndrome 13 2 0.010 None 1.000 1 2017 2017
CUI: C1855067
Disease: B lymphocytopenia
B lymphocytopenia
phenotype Immune System Diseases; Hemic and Lymphatic Diseases Finding 13 0.100 None 0
CUI: C0023786
Disease: Mucopolysaccharidosis I
Mucopolysaccharidosis I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 16 31 0.010 None 1.000 1 2013 2013
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections
phenotype Finding 16 0.100 None 0
Recurrent infection of the gastrointestinal tract
phenotype Finding 16 0.100 None 0
CUI: C4021020
Disease: Non-midline cleft lip
Non-midline cleft lip
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 16 0.100 None 0
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 17 3 0.010 None 1.000 1 2017 2017
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
disease Neoplastic Process 17 1 0.010 None 1.000 1 2003 2003
Advanced Head and Neck Squamous Cell Carcinoma
disease Neoplastic Process 17 0.010 None 1.000 1 2010 2010
CUI: C2931322
Disease: T-Lymphocytopenia
T-Lymphocytopenia
disease Immune System Diseases; Hemic and Lymphatic Diseases Finding 17 0.100 None 0
CUI: C1303073
Disease: Nicolaides Baraitser syndrome
Nicolaides Baraitser syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 18 38 0.320 limited 1.000 3 1985 2019
CUI: C0281842
Disease: Abnormality of the fallopian tube
Abnormality of the fallopian tube
phenotype Anatomical Abnormality 22 0.100 None 0
CUI: C0024776
Disease: Maple Syrup Urine Disease
Maple Syrup Urine Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 24 134 0.010 None 1.000 1 2017 2017