microphakia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal smallness of the lens. (Human Phenotype Ontology, HP_0012376)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012376
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Genes

2 genes associated with the microphakia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HMX1 H6 family homeobox 1
LMX1B LIM homeobox transcription factor 1, beta