abnormal renal corticomedullary differentiation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of corticomedullary differentiation (CMD) on diagnostic imaging such as magnetic resonance imaging, computer tomography, or sonography. CMD is a difference in the visualization of cortex and medulla. (Human Phenotype Ontology, HP_0005932)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005932
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4 genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit
INVS inversin
NIPBL Nipped-B homolog (Drosophila)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)