S100B, S100 calcium binding protein B, 6285

N. diseases: 599; N. variants: 6
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.
Familial Hemophagocytic Lymphocytosis
phenotype Hemic and Lymphatic Diseases Disease or Syndrome 35 6 0.010 None 1.000 1 1986 1986
Asymptomatic human immunodeficiency virus infection
disease Infections; Immune System Diseases Disease or Syndrome 26 0.010 None 1.000 1 1989 1989
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 84 4 0.010 None 1.000 1 1990 1990
CUI: C0026277
Disease: Mixed Salivary Gland Tumor
Mixed Salivary Gland Tumor
disease Neoplasms Neoplastic Process 185 3 0.010 None 1.000 1 1991 1991
CUI: C0686377
Disease: CNS metastases
CNS metastases
phenotype Neoplasms; Nervous System Diseases Neoplastic Process 102 14 0.010 None 1.000 1 1991 1991
Chronic lymphoproliferative disease NOS
disease Neoplastic Process 3 0.010 None 1.000 1 1991 1991
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis
disease Neoplasms Disease or Syndrome 18 10 0.010 None < 0.001 1 1992 1992
CUI: C0026499
Disease: Monosomy
Monosomy
group Pathological Conditions, Signs and Symptoms Congenital Abnormality 214 11 0.010 None 1.000 1 1992 1992
CUI: C0795875
Disease: Chromosome 21 monosomy
Chromosome 21 monosomy
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 13 0.010 None 1.000 1 1992 1992
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis
disease Neoplasms Neoplastic Process 19 7 0.010 None < 0.001 1 1992 1992
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Mental or Behavioral Dysfunction 1263 112 0.020 None 1.000 2 1993 1993
CUI: C0023492
Disease: Leukemia, T-Cell
Leukemia, T-Cell
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 457 10 0.020 None 1.000 2 1988 1993
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction
disease Nervous System Diseases Disease or Syndrome 45 0.010 None 1.000 1 1993 1993
CUI: C0023493
Disease: Adult T-Cell Lymphoma/Leukemia
Adult T-Cell Lymphoma/Leukemia
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 540 11 0.010 None 1.000 1 1993 1993
CUI: C0024314
Disease: Lymphoproliferative Disorders
Lymphoproliferative Disorders
group Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 300 14 0.020 None 1.000 2 1991 1994
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases Disease or Syndrome 852 704 0.010 None 1.000 1 1994 1994
CUI: C4048329
Disease: Immunosuppression
Immunosuppression
disease Disease or Syndrome 632 9 0.010 None 1.000 1 1996 1996
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases
group Digestive System Diseases Disease or Syndrome 144 14 0.010 None 1.000 1 1996 1996
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex
disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 4 0.010 None < 0.001 1 1998 1998
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor
disease Neoplasms Neoplastic Process 95 1 0.010 None 1.000 1 1999 1999
CUI: C1266175
Disease: Parachordoma
Parachordoma
disease Neoplasms Neoplastic Process 3 0.010 None 1.000 1 1999 1999
Ewings sarcoma-primitive neuroectodermal tumor (PNET)
disease Neoplasms Neoplastic Process 117 3 0.010 None 1.000 1 1999 1999
CUI: C1141957
Disease: HIV disease progression
HIV disease progression
disease Disease or Syndrome 54 5 0.020 None 1.000 2 1995 2000
CUI: C1334455
Disease: Pulmonary Sclerosing Hemangioma
Pulmonary Sclerosing Hemangioma
disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 33 3 0.010 None < 0.001 1 2000 2000
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
disease Digestive System Diseases Disease or Syndrome 1382 1147 0.010 None 1.000 1 2001 2001