albuminuria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of albumin in the urine, an indicator of KIDNEY DISEASES. (Experimental Factor Ontology, EFO_0004285)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012592
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Genes

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

Symbol Name
PEX1 peroxisomal biogenesis factor 1