weill-marchesani syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities. (Human Disease Ontology, DOID_0050475)
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Genes

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

Symbol Name Standardized Value
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10 2.81527
ADAMTSL2 ADAMTS-like 2 2.33704
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17 2.31276
FBN1 fibrillin 1 2.26428
ADAMTSL4 ADAMTS-like 4 2.06442
LTBP3 latent transforming growth factor beta binding protein 3 1.67141
TBRG1 transforming growth factor beta regulator 1 1.6543
LTBP2 latent transforming growth factor beta binding protein 2 1.62739
PAPLN papilin, proteoglycan-like sulfated glycoprotein 1.56311
FBN3 fibrillin 3 1.30488
ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif, 20 1.24515
SUOX sulfite oxidase 1.21998
MMP25 matrix metallopeptidase 25 0.955361
FBN2 fibrillin 2 0.891308
LTBP1 latent transforming growth factor beta binding protein 1 0.889668
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1 0.681096
ADAMTS4 ADAM metallopeptidase with thrombospondin type 1 motif, 4 0.566831
FURIN furin (paired basic amino acid cleaving enzyme) 0.40904
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 0.311014
TGFBR2 transforming growth factor, beta receptor II (70/80kDa) 0.227642
CBS cystathionine-beta-synthase 0.201308
SMAD4 SMAD family member 4 0.200006
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 0.187415
SMAD2 SMAD family member 2 0.180937