Semilobar Holoprosencephaly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of holoprosencephaly in which the left and right frontal and parietal lobes are fused and the interhemispheric fissure is only present posteriorly. (Human Phenotype Ontology, HP_0002507)
External Link https://www.disgenet.org/browser/0/1/0/C0751617
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Genes

17 genes associated with the disease Semilobar Holoprosencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CDON cell adhesion associated, oncogene regulated
CNOT1 CCR4-NOT transcription complex, subunit 1
DISP1 dispatched homolog 1 (Drosophila)
DLL1 delta-like 1 (Drosophila)
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FOXH1 forkhead box H1
GAS1 growth arrest-specific 1
GLI2 GLI family zinc finger 2
NODAL nodal growth differentiation factor
PTCH1 patched 1
SHH sonic hedgehog
SIX3 SIX homeobox 3
TDGF1 teratocarcinoma-derived growth factor 1
TGIF1 TGFB-induced factor homeobox 1
TWSG1 twisted gastrulation BMP signaling modulator 1
ZIC2 Zic family member 2