abnormality of the nasal skeleton Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the nasal skeleton. (Human Phenotype Ontology, HP_0010937)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010937
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1 genes associated with the abnormality of the nasal skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
USH1G Usher syndrome 1G (autosomal recessive)