midline defect of the nose Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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 http://compbio.charite.de/hpoweb/showterm?id=HP:0004122
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14 genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX4 ALX homeobox 4
BCOR BCL6 corepressor
EFNB1 ephrin-B1
FAM58A family with sequence similarity 58, member A
FRAS1 Fraser extracellular matrix complex subunit 1
FREM1 FRAS1 related extracellular matrix 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
HYLS1 hydrolethalus syndrome 1
NF1 neurofibromin 1
PTCH1 patched 1
TBX2 T-box 2
TBX4 T-box 4
ZSWIM6 zinc finger, SWIM-type containing 6