Weill-Marchesani Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
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)
External Link https://www.disgenet.org/browser/0/1/0/C1869114
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Genes

6 genes associated with the disease Weill-Marchesani Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17
CERS3 ceramide synthase 3
FBN1 fibrillin 1
LTBP2 latent transforming growth factor beta binding protein 2
MFAP1 microfibrillar-associated protein 1