writing disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A learning disability that involves impaired written language ability such as impairments in handwriting, spelling, organization of ideas, and composition. (Human Disease Ontology, DOID_0060047)
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23 genes co-occuring with the disease writing disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
COPS2 COP9 signalosome subunit 2 1.5093
PNMA2 paraneoplastic Ma antigen 2 1.31537
DCDC2 doublecortin domain containing 2 1.12193
MAP4K5 mitogen-activated protein kinase kinase kinase kinase 5 1.08244
LSR lipolysis stimulated lipoprotein receptor 1.03746
MYBPC1 myosin binding protein C, slow type 1.0244
DEDD death effector domain containing 0.9696
CAMP cathelicidin antimicrobial peptide 0.88434
CBS cystathionine-beta-synthase 0.806488
PRNP prion protein 0.788442
TES testin LIM domain protein 0.660404
CCL20 chemokine (C-C motif) ligand 20 0.564889
MBP myelin basic protein 0.541217
MAPT microtubule-associated protein tau 0.528835
GRN granulin 0.527676
CD6 CD6 molecule 0.493503
MAPK14 mitogen-activated protein kinase 14 0.412405
TBX1 T-box 1 0.408666
APOH apolipoprotein H (beta-2-glycoprotein I) 0.354499
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 0.347511
LSS lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase) 0.301254
F5 coagulation factor V (proaccelerin, labile factor) 0.192971
ACHE acetylcholinesterase (Yt blood group) 0.163111