abnormality of the ciliary body Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A structural anomaly of the ciliary body (FMA:58295). (Human Phenotype Ontology, HP_0012776)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012776
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Genes

1 genes associated with the abnormality of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LAMB2 laminin, beta 2 (laminin S)