impaired renal concentrating ability Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A defect in the ability to concentrate the urine. (Human Phenotype Ontology, HP_0004727)
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3 genes associated with the impaired renal concentrating ability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CEP290 centrosomal protein 290kDa
FAM20A family with sequence similarity 20, member A
HBB hemoglobin, beta