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Article

Validating a Computable Phenotype for Nephrotic Syndrome in Children and Adults Using PCORnet Data.

Kidney360 - 30 Dec 2021

Oliverio Andrea L, Marchel Dorota, Troost Jonathan P, Ayoub Isabelle, Almaani Salem, Greco Jessica, Tran Cheryl L, Denburg Michelle R, Matheny Michael, Dorn Chad, Massengill Susan F, Desmond Hailey, Gipson Debbie S, Mariani Laura H

Abstract excerpt

Background: Primary nephrotic syndromes are rare diseases which can impede adequate sample size for observational patient-oriented research and clinical trial enrollment. A computable phenotype may be powerful in identifying patients with these diseases for research across multiple institutions. Methods: A comprehensive algorithm of inclusion and exclusion ICD-9 and ICD-10 codes to identify patients with primary...

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Identifiers

PMID: 35419531
DOI: 10.34067/KID.0002892021
PMCID: PMC8986057

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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