Holoprosencephaly Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. (Human Disease Ontology, DOID_4621)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D016142
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Genes

9 genes/proteins associated with the disease Holoprosencephaly from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
TDGF1	teratocarcinoma-derived growth factor 1	2.88009
TWSG1	twisted gastrulation BMP signaling modulator 1	2.88009
NODAL	nodal growth differentiation factor	2.88009
HPE1	holoprosencephaly 1, alobar	2.88009
HPE6	holoprosencephaly 6	2.88009
SHH	sonic hedgehog	2.88009
SIX3	SIX homeobox 3	2.88009
GAS1	growth arrest-specific 1	2.88009
TGIF1	TGFB-induced factor homeobox 1	2.88009