Human Gene Set: HP_ABNORMAL_RENAL_CORTICOMEDULLARY_DIFFERENTIATION


Standard name HP_ABNORMAL_RENAL_CORTICOMEDULLARY_DIFFERENTIATION
Systematic name M36781
Brief description Abnormal renal corticomedullary differentiation
Full description or abstract 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. [https://orcid.org/0000-0002-0736-9199, PMID:22528889]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0005932
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0005932
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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