holoprosencephaly Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
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)
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Genes

18 genes co-occuring with the biological term holoprosencephaly in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
APOB	apolipoprotein B
APOE	apolipoprotein E
CDON	cell adhesion associated, oncogene regulated
DLL1	delta-like 1 (Drosophila)
FBXW11	F-box and WD repeat domain containing 11
FGF8	fibroblast growth factor 8 (androgen-induced)
FOXH1	forkhead box H1
GAS1	growth arrest-specific 1
GLI2	GLI family zinc finger 2
NODAL	nodal growth differentiation factor
NOG	noggin
NOTCH1	notch 1
SHH	sonic hedgehog
SIX3	SIX homeobox 3
STIL	SCL/TAL1 interrupting locus
TGIF1	TGFB-induced factor homeobox 1
TWSG1	twisted gastrulation BMP signaling modulator 1
ZIC2	Zic family member 2