FUS, FUS RNA binding protein, 2521

N. diseases: 301; N. variants: 39
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: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.100 None 1.000 26 1 2010 2018
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
disease Disease or Syndrome 27 67 0.430 None 1.000 16 16 2009 2016
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
disease Disease or Syndrome 138 21 0.100 None 1.000 14 1 2009 2019
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
TREMOR, HEREDITARY ESSENTIAL, 4
disease Disease or Syndrome 1 4 0.600 None 1.000 10 4 2009 2014
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.050 None 1.000 5 2004 2018
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
disease Disease or Syndrome 8 23 0.020 None 1.000 2 2011 2013
Human immunodeficiency virus (HIV) II infection category B1
disease Disease or Syndrome 985 56 0.020 None 1.000 2 2019 2019
CUI: C0220613
Disease: Adult Soft Tissue Sarcoma
Adult Soft Tissue Sarcoma
disease Neoplastic Process 162 3 0.010 None 1.000 1 2012 2012
CUI: C0220645
Disease: Childhood Soft Tissue Sarcoma
Childhood Soft Tissue Sarcoma
disease Neoplastic Process 166 3 0.010 None 1.000 1 2012 2012
CUI: C0279068
Disease: Childhood Solid Neoplasm
Childhood Solid Neoplasm
phenotype Neoplastic Process 169 3 0.010 None 1.000 1 2000 2000
CUI: C0280099
Disease: Adult Solid Neoplasm
Adult Solid Neoplasm
group Neoplastic Process 163 3 0.010 None 1.000 1 2000 2000
CUI: C0334070
Disease: Maturation defect
Maturation defect
phenotype Acquired Abnormality 43 2 0.010 None 1.000 1 2019 2019
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease
disease Disease or Syndrome 18 7 0.010 None 1.000 1 2017 2017
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
disease Neoplastic Process 860 154 0.010 None 1.000 1 2010 2010
CUI: C0876991
Disease: Histiocytosis haematophagic
Histiocytosis haematophagic
disease Disease or Syndrome 36 2 0.010 None 1.000 1 2010 2010
CUI: C1510420
Disease: Cavitation
Cavitation
disease Anatomical Abnormality 47 0.010 None 1.000 1 2019 2019
Low Grade Fibromyxoid Sarcoma with Giant Collagen Rosettes
disease Neoplastic Process 2 0.010 None 1.000 1 2007 2007
Non-Metastatic Childhood Soft Tissue Sarcoma
disease Neoplastic Process 160 3 0.010 None 1.000 1 2012 2012
CUI: C4020732
Disease: Mitochondrial abnormalities
Mitochondrial abnormalities
disease Anatomical Abnormality 83 20 0.010 None 1.000 1 2015 2015
CUI: C4087469
Disease: Myxoid liposarcoma metastatic
Myxoid liposarcoma metastatic
disease Neoplastic Process 3 0.010 None 1.000 1 2016 2016
CUI: C4225412
Disease: Spondylo-ocular syndrome
Spondylo-ocular syndrome
disease Disease or Syndrome 24 5 0.010 None 1.000 1 2018 2018
CUI: C4324336
Disease: Hyperleukocytosis
Hyperleukocytosis
disease Disease or Syndrome 21 0.010 None 1.000 1 2020 2020
Non-ST-segment elevation myocardial infarction (NSTEMI)
disease Disease or Syndrome 18 1 0.010 None 1.000 1 2019 2019
CUI: C4727003
Disease: Unresectable Soft Tissue Sarcoma
Unresectable Soft Tissue Sarcoma
disease Neoplastic Process 2 0.010 None 1.000 1 2016 2016
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
phenotype Finding 218 11 0.100 None 0