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Details
Link-It Detail - Human Phenotype - Abnormal renal corticomedullary differentiation
Debug Stats
  • ### Total Build Time: 20 ms 16.904 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 222 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 368 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 1.090 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.151 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 7.689 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 5.212 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.041 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal renal corticomedullary differentiation HP:0005932
Definition (1)
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.
Parents (3)
img Abnormality of the renal cortex HP:0011035
img Abnormality of the renal medulla HP:0100957
img Abnormality of the kidney HP:0000077
Children (3)
img Reduced renal corticomedullary differentiation HP:0005565
img Loss of definition of corticomedullary differentiation HP:0005573
img Absence of renal corticomedullary differentiation HP:0005564
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the renal cortex HP:0011035
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the renal cortex HP:0011035
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the renal cortex HP:0011035
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the renal medulla HP:0100957
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the renal medulla HP:0100957
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the renal medulla HP:0100957
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the kidney HP:0000077
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the kidney HP:0000077
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanINVS27130inversin
img HP RolledUp, OMIM ID: 602088
HumanNIPBL25836Nipped-B homolog (Drosophila)
img HP RolledUp, OMIM ID: 122470
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img HP RolledUp, OMIM ID: 602522
HumanPKHD15314polycystic kidney and hepatic disease 1 (autosomal recessive)
img HP RolledUp, OMIM ID: 263200
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img HP RolledUp, OMIM ID: 602522
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img HP RolledUp, OMIM ID: 602522
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005932Abnormal renal corticomedullary differentiation0self