Attention-Deficit hyperactivity disorder (ADHD)
A. John, Y. Friedmann, M. DelPozo-Banos, A. Frizzati, T. Ford, A. Thapar
PH932 / 3535 Clinical-Coded Phenotype
Overview
Phenotype TypeDisease or syndromeSexBothValid Event Date RangeNo dataCoding SystemSNOMED CT codesICD10 codesRead codes v2CollectionsAdolescent Data Platform (ADP)DATAMINDPhenotype LibraryTagsNo dataDefinition
Attention-Deficit hyperactivity disorder (ADHD) is a neurodevelopmental condition with secondary behavioural, social, and educational difficulties. ADHD is defined as a behavioural syndrome characterized by the core symptoms of hyperactivity, impulsivity, and inattention which can lead to psychological, social, education, or occupational impairment. The ADHD phenotype includes hyperkinetic disorder, hyperkinetic conduct disorder, attention-deficit hyperactivity disorder and disturbance of activity and attention.
ICD-10 definition
This definition has been previously validated and published (John et al, 2022; Martin et al, 2024).
Read codes definition
This definition also includes disturbance of activity and attention, attention deficit with/without hyperactivity, and ADHD treatment, management and monitoring. This definition has been previously validated and published (John et al, 2022; Martin et al, 2024).
SNOMED CT definition
This definition has been created by mapping the existing Read code and ICD-10 definitions and additional exploration of SNOMED CT codes. It excludes non-specific definitions of neurodevelopmental disorders, developmental delay, attentional delay and measurement codes for ADHD medication/prescription.
An auxiliary concept “ADHD assessments” is provided to help identify individuals being assessed for ADHD.
Warning: The SNOMED CT definition have not undergone validation yet.
References
John, A., Friedmann, Y., DelPozo-Banos, M., Frizzati, A., Ford, T., & Thapar, A. (2022). Association of school absence and exclusion with recorded neurodevelopmental disorders, mental disorders, or self-harm: a nationwide, retrospective, electronic cohort study of children and young people in Wales, UK. The Lancet Psychiatry, 9(1), 23-34.
Martin, J., Langley, K., Cooper, M., Rouquette, O.Y., John, A., Sayal, K., Ford, T. and Thapar, A. (2024). Sex differences in attention-deficit hyperactivity disorder diagnosis and clinical care: a national study of population healthcare records in Wales. J Child Psychol Psychiatr.
Implementation
Implementation
Clinical Code List
PUBLISHED - 98 Codes
PUBLISHED - 7 Codes
PUBLISHED - 230 Codes
Publication
John,A., Friedmann, Y., DelPozo-Banos, M., Frizzati, A., Ford, T., & Thapar, A.(2022). Association of school absence and exclusion with recorded neurodevelopmental disorders, mental disorders, or self-harm: a nationwide, retrospective, electronic cohort study of children and young people in Wales, UK. The Lancet Psychiatry. Volume 9, Issue 1,2022,Pages 23-34,ISSN 2215-0366, https://doi.org/10.1016/S2215-0366(21)00367-9
(DOI:10.1016/S2215-0366(21)00367-9)
Citation Requirements
John, A., Friedmann, Y., DelPozo-Banos, M., Frizzati, A., Ford, T., & Thapar, A. (2022). Association of school absence and exclusion with recorded neurodevelopmental disorders, mental disorders, or self-harm: a nationwide, retrospective, electronic cohort study of children and young people in Wales, UK. The Lancet Psychiatry, 9(1), 23-34.
Citation Example
A. John, Y. Friedmann, M. DelPozo-Banos, A. Frizzati, T. Ford, A. Thapar. PH932 / 3535 - Attention-Deficit hyperactivity disorder (ADHD). Phenotype Library [Online]. 23 July 2024. Available from: http://phenotypes.healthdatagateway.org/phenotypes/PH932/version/3535/detail/. [Accessed 23 November 2024]
API
To Export Phenotype Details:
Format API JSON site_root/api/v1/phenotypes/PH932/version/3535/detail/?format=json R Package library(ConceptLibraryClient)
# Connect to API
client = ConceptLibraryClient::Connection$new(public=TRUE)
# Get details of phenotype
phenotype_details = client$phenotypes$get_detail(
'PH932',
version_id=3535
)Py Package from pyconceptlibraryclient import Client
# Connect to API
client = Client(public=True)
# Get codelist of phenotype
phenotype_codelist = client.phenotypes.get_detail(
'PH932',
version_id=3535
)To Export Phenotype Code List:
Format API JSON site_root/api/v1/phenotypes/PH932/version/3535/export/codes/?format=json CSV site_root/phenotypes/PH932/version/3535/export/codes/ R Package library(ConceptLibraryClient)
# Connect to API
client = ConceptLibraryClient::Connection$new(public=TRUE)
# Get codelist of phenotype
phenotype_codelist = client$phenotypes$get_codelist(
'PH932',
version_id=3535
)Py Package from pyconceptlibraryclient import Client
# Connect to API
client = Client(public=True)
# Get codelist of phenotype
phenotype_codelist = client.phenotypes.get_codelist(
'PH932',
version_id=3535
)Version History