pfeiffer syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An acrocephalosyndactylia that has_material_basis_in mutations in the FGFR1 and FGFR2 gene which results_in premature fusion located_in skull. (Human Disease Ontology, DOID_14705)
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Genes

20 genes co-occuring with the disease pfeiffer syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FGFR2 fibroblast growth factor receptor 2 2.82341
FGFR1 fibroblast growth factor receptor 1 2.16969
FGFR3 fibroblast growth factor receptor 3 1.76728
FGF10 fibroblast growth factor 10 0.8741
RAB23 RAB23, member RAS oncogene family 0.808539
MSX2 msh homeobox 2 0.795821
TWIST1 twist family bHLH transcription factor 1 0.666358
FGF7 fibroblast growth factor 7 0.646559
VPREB1 pre-B lymphocyte 1 0.621008
FGF9 fibroblast growth factor 9 0.567609
FGF1 fibroblast growth factor 1 (acidic) 0.552075
FLNB filamin B, beta 0.545868
FGF8 fibroblast growth factor 8 (androgen-induced) 0.397843
MSX1 msh homeobox 1 0.396725
FGF4 fibroblast growth factor 4 0.389281
MTM1 myotubularin 1 0.350452
SPARC secreted protein, acidic, cysteine-rich (osteonectin) 0.229716
CTSK cathepsin K 0.214975
C6ORF25 chromosome 6 open reading frame 25 0.195183
MNX1 motor neuron and pancreas homeobox 1 0.166768