aplasia/hypoplasia of the nasal septum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the nasal septum. (Human Phenotype Ontology, HP_0009935)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009935
Similar Terms
Downloads & Tools

Genes

5 genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLNB filamin B, beta
NOG noggin
PTCH1 patched 1
SIX3 SIX homeobox 3
TGIF1 TGFB-induced factor homeobox 1