Midline Defect Of The Nose Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description This term groups together three conditions that presumably represent different degrees of severity of a midline defect of the nose or nasal tip. (Human Phenotype Ontology, HP_0004122)
External Link https://www.disgenet.org/browser/0/1/0/C4025411
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Genes

4 genes associated with the disease Midline Defect Of The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
EFNB1 ephrin-B1
LONP1 lon peptidase 1, mitochondrial
PTCH1 patched 1
ZSWIM6 zinc finger, SWIM-type containing 6