Marden-Walker Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Marden-Walker syndrome (MWS) is a malformation syndrome characterized by multiple joint contractures (arthrogryposis), a mask-like face with blepharophimosis, micrognathia, high-arched or cleft palate, low-set ears, decreased muscular bulk, kyphoscoliosis and arachnodactyly. (Orphanet Rare Disease Ontology, Orphanet_2461)
External Link	https://www.disgenet.org/browser/0/1/0/C0796033
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Genes

8 genes associated with the disease Marden-Walker Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CHST14	carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
GEMIN2	gem (nuclear organelle) associated protein 2
NLRP3	NLR family, pyrin domain containing 3
PIEZO2	piezo-type mechanosensitive ion channel component 2
RET	ret proto-oncogene
SCAF11	SR-related CTD-associated factor 11
SLC9A3R2	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2
ZEB2	zinc finger E-box binding homeobox 2