Bifid Nose Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Visually assessable vertical indentation, cleft, or depression of the nasal bridge, ridge and tip. (Human Phenotype Ontology, HP_0011803)
External Link https://www.disgenet.org/browser/0/1/0/C0221363
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Genes

9 genes associated with the disease Bifid Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
ALX3 ALX homeobox 3
ALX4 ALX homeobox 4
FREM1 FRAS1 related extracellular matrix 1
HYLS1 hydrolethalus syndrome 1
NF1 neurofibromin 1
TBX4 T-box 4
ZIC2 Zic family member 2
ZSWIM6 zinc finger, SWIM-type containing 6