| 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 |
| Similar Terms | |
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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.
