Mowat-Wilson Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR; see this term) and variable congenital malformations. (Orphanet Rare Disease Ontology, Orphanet_2152)
External Link	https://www.disgenet.org/browser/0/1/0/C1856113
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Genes

10 genes associated with the disease Mowat-Wilson Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ARSD	arylsulfatase D
GEMIN2	gem (nuclear organelle) associated protein 2
HOXA6	homeobox A6
MEF2C	myocyte enhancer factor 2C
PHOX2B	paired-like homeobox 2b
POGZ	pogo transposable element with ZNF domain
SCAF11	SR-related CTD-associated factor 11
SLC9A3R2	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2
SOX10	SRY (sex determining region Y)-box 10
ZEB2	zinc finger E-box binding homeobox 2