Chronic kidney disease (Phenotype)

Synonyms:HP:0000106, HP:0001918, HP:0008671, Chronic kidney disease, CKD
Id:HP:0012622
Description:Functional anomaly of the kidney persisting for at least three months.
Results found

Linked to

 

Label

Description

 

Subject

A subject from Metabolomics produced as part of the PR001042 project

Gene

corin, serine peptidase

Gene

BTG anti-proliferation factor 1

Gene

cystinosin, lysosomal cystine transporter

Gene

TP53RK binding protein

Gene

HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]

Gene

aldolase, fructose-bisphosphate B

Gene

advillin

Gene

HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]

Gene

lactate dehydrogenase A [Source:HGNC Symbol;Acc:HGNC:6535]

  • Subject

    A subject from Metabolomics produced as part of the PR001042 project


  • Gene

    corin, serine peptidase


  • Gene

    BTG anti-proliferation factor 1


  • Gene

    cystinosin, lysosomal cystine transporter


  • Gene

    TP53RK binding protein


  • Gene

    HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]


  • Gene

    aldolase, fructose-bisphosphate B



  • Gene

    HECT and RLD domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:HGNC:4868]


  • Gene

    lactate dehydrogenase A [Source:HGNC Symbol;Acc:HGNC:6535]

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