abnormality of threonine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of a threonine metabolic process. (Human Phenotype Ontology, HP_0010900)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010900
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Genes

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

Symbol Name
GUCY2D guanylate cyclase 2D, membrane (retina-specific)