Neonatal jaundice (excl haemolytic dz of the newborn)
Kuan V, Denaxas S, Gonzalez-Izquierdo A, Direk K, Bhatti O, Husain S, Sutaria S, Hingorani M, Nitsch D, Parisinos C, Lumbers T, Mathur R, Sofat R, Casas JP, Wong I, Hemingway H, Hingorani A
PH217 / 434 Clinical-Coded Phenotype
Overview
Phenotype TypeDisease or syndromePhenotype UUIDMEqZPyc5s3rBZqLaCnkMfBSexBothValid Event Date Range01/01/1999 - 01/07/2016Coding SystemICD10 codesRead codes v2Med codesData SourcesCollectionsCALIBERPhenotype LibraryTagsNo dataDefinition
At the specified date, a patient is defined as having had 'Neonatal jaundice (excl haemolytic dz of the newborn)' (excl haemolytic dz of the newborn) IF they meet the criteria for any of the following on or before the specified date. The earliest date on which the individual meets any of the following criteria on or before the specified date is defined as the first event date:
Primary care
'Neonatal jaundice (excl haemolytic dz of the newborn)' (excl haemolytic dz of the newborn) diagnosis or history of diagnosis during a consultation AND IF the patient is aged < 1y at the first event date OR Secondary care
ALL diagnoses of 'Neonatal jaundice (excl haemolytic dz of the newborn)' (excl haemolytic dz of the newborn) or history of diagnosis during a hospitalization AND IF the patient is aged < 1y at the first event date
Implementation
Implementation
Clinical Code List
PUBLISHED - 45 Codes
PUBLISHED - 45 Codes
PUBLISHED - 2 Codes
Publication
Kuan V., Denaxas S., Gonzalez-Izquierdo A. et al. A chronological map of 308 physical and mental health conditions from 4 million individuals in the National Health Service. The Lancet Digital Health - DOI 10.1016/S2589-7500(19)30012-3
(DOI:10.1016/S2589-7500(19)30012-3)
Citation Example
Kuan V, Denaxas S, Gonzalez-Izquierdo A, Direk K, Bhatti O, Husain S, Sutaria S, Hingorani M, Nitsch D, Parisinos C, Lumbers T, Mathur R, Sofat R, Casas JP, Wong I, Hemingway H, Hingorani A. PH217 / 434 - Neonatal jaundice (excl haemolytic dz of the newborn). Phenotype Library [Online]. 06 October 2021. Available from: http://phenotypes.healthdatagateway.org/phenotypes/PH217/version/434/detail/. [Accessed 08 September 2024]
API
To Export Phenotype Details:
Format API JSON site_root/api/v1/phenotypes/PH217/version/434/detail/?format=json R Package library(ConceptLibraryClient)
# Connect to API
client = ConceptLibraryClient::Connection$new(public=TRUE)
# Get details of phenotype
phenotype_details = client$phenotypes$get_detail(
'PH217',
version_id=434
)Py Package from pyconceptlibraryclient import Client
# Connect to API
client = Client(public=True)
# Get codelist of phenotype
phenotype_codelist = client.phenotypes.get_detail(
'PH217',
version_id=434
)To Export Phenotype Code List:
Format API JSON site_root/api/v1/phenotypes/PH217/version/434/export/codes/?format=json CSV site_root/phenotypes/PH217/version/434/export/codes/ R Package library(ConceptLibraryClient)
# Connect to API
client = ConceptLibraryClient::Connection$new(public=TRUE)
# Get codelist of phenotype
phenotype_codelist = client$phenotypes$get_codelist(
'PH217',
version_id=434
)Py Package from pyconceptlibraryclient import Client
# Connect to API
client = Client(public=True)
# Get codelist of phenotype
phenotype_codelist = client.phenotypes.get_codelist(
'PH217',
version_id=434
)Version History