aplasia/hypoplasia of the choroid Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the choroid. (Human Phenotype Ontology, HP_0001122)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001122
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1 genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TRIM37 tripartite motif containing 37