Glomerular Disease

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dc.contributor.authorGoodwin Davies, Amy
dc.contributor.authorMarchesani, Nicole
dc.contributor.otherChildren's Hospital of Philadelphia
dc.contributor.otherPEDSnet Data Coordinating Center
dc.date.accessioned2025-06-03T14:45:12Z
dc.date.created2024-11
dc.descriptionThe glomerular disease computable phenotype will identify a cohort of patients meeting criteria for glomerular disease based on criteria developed as part of the GLEAN study. ##### Inclusion Criteria Broad pathways into the cohort: - 2 or more glomerular inclusion diagnoses on different dates OR - 1 or more glomerular inclusion diagnoses AND 1 or more kidney biopsy which is not post-transplant Inclusion diagnoses with special requirements: - 1 or more "other_code_req" diagnosis AND 1 or more additional glomerular inclusion diagnosis on a different date OR 1 or more kidney biopsy that is not post-transplant - 1 or more `neph_req` diagnosis that is associated with a nephrology visit ##### Exclusion Criteria - Inclusion events occur after `age_ub_years` (defaults to 30), before the minimum date cutoff or after the maximum date cutoff, or after the patient's endpoint date - Kidney biopsy occurs after a kidney transplant.
dc.description.abstractA phenotype for identifying patients with glomerular disease based on diagnoses and kidney biopsy procedures. Downloadable content for this Phenotype includes two R files (cohorts.R and driver.R) and a specs folder, which includes the required concept sets.
dc.identifier.urihttps://hdl.handle.net/20.500.14642/1054
dc.provenanceDeveloped as part of the Preserving Kidney Function in Children with Chronic Kidney Disease (PRESERVE) study.
dc.publisherPEDSnet
dc.relationKidney Transplant
dc.relationKidney Biopsy
dc.relationGlomerular Disease
dc.relation.urihttps://github.com/PRESERVE-Coordinating-Center/PRESERVE_Variables/blob/main/analytic_code/glomerular_phenotype.R
dc.rightsa CC-BY Attribution 4.0 license.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectPCORnet Data Model
dc.subject.meshGlomerulonephritis
dc.subject.meshNephritis
dc.subject.meshKidney Diseases
dc.subject.meshUrologic Diseases
dc.subject.otherCPT4
dc.subject.otherHCPCS
dc.subject.otherICD-9-Proc
dc.subject.otherICD-10-PCS
dc.subject.otherSNOMED
dc.subject.otherICD-9
dc.subject.otherICD-10
dc.subject.otherICD-10-CM
dc.titleGlomerular Disease
dspace.entity.typePhenotype
local.quality.statusResearch-Ready
local.subject.flatAny Age Patient Population
local.subject.flatAny Gender Identity Patient Population
local.subject.flatAny Race/Ethnicity Patient Population
local.subject.flatPCORnet Data Model
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relation.isConceptSetOfPhenotypeef0d5b01-14ab-4173-b18e-6dc83861cc59
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relation.isConceptSetOfPhenotype.latestForDiscovery9387a531-2126-4989-976b-699d90533f13
relation.isDocumentationOfPhenotypefc7538fd-56d6-44da-96b1-22b9c8fda34e
relation.isDocumentationOfPhenotype.latestForDiscoveryfc7538fd-56d6-44da-96b1-22b9c8fda34e
relation.isStudyOfPhenotype6df51ca1-7a01-4551-b1f1-ca70aaf2c5ae
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Diagnosis Phenotypes