FB2024_03 , released June 25, 2024
Human Disease Model Report: attention deficit hyperactivity disorder, susceptibility to
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General Information
Name
attention deficit hyperactivity disorder, susceptibility to
FlyBase ID
FBhh0000653
Disease Ontology Term
Parent Disease
Overview

This report describes the general characteristics of attention deficit hyperactivity disorder (ADHD), which is estimated to affect 5-7% of children and adolescents worldwide. ADHD is a complex multifactorial disorder involving both genetic susceptibility and environmental triggers; multiple susceptibility loci have been identified (see MIM:143465). Heritability of ADHD is estimated to be in the range of 60-80%.

For putative susceptibility loci studied using Drosophila models, see the "Related Diseases" section below.

For a number of diseases that are associated with increased incidence of symptoms of ADHD, that aspect of the disease has been investigated in flies; see neurofibromatosis, type 1 (FBhh0000197) and Alzheimer disease 1 (FBhh0000119).

[updated Nov. 2017 by FlyBase; FBrf0222196]

Disease Summary Information
Parent Disease Summary: attention deficit hyperactivity disorder, susceptibility to
OMIM report

[ATTENTION DEFICIT-HYPERACTIVITY DISORDER; ADHD](https://omim.org/entry/143465)

Symptoms and phenotype

Meta-regression analyses have estimated the worldwide ADHD/HKD prevalence at between 5.3% and 7.1% in children and adolescents, and at 3.4% (range 1.2-7.3%) in adults (http://adhd-institute.com/burden-of-adhd/epidemiology/).

Attention-deficit/hyperactivity disorder (ADHD) is a chronic condition that includes a combination of persistent problems, such as difficulty sustaining attention, hyperactivity and impulsive behavior; the condition often continues into adulthood (https://www.mayoclinic.org/diseases-conditions/adhd/symptoms-causes/syc-20350889).

ADHD is the most common childhood-onset behavioral disorder, affecting approximately 5 to 10% of children and adolescents (Wolraich et al., 1996; pubmed: 8714320). In this condition, persistent inattention and/or hyperactive-impulsive behavior results in impaired social and/or academic functioning. Boys are affected about 8 times more frequently than girls (Zametkin et al., 1990; pubmed:2233902). [from MIM:143465; 2017.11.21]

Genetics

Twin studies estimate the heritability of ADHD to be 70-80% (reviewed in Matthews, et al., 2014; pubmed:24214656 ); other estimates are in the range of 60-75% (reviewed in Cortese, 2012; pubmed:22306277).

Multiple genes contribute to the phenotype of attention deficit-hyperactivity disorder. [from MIM:143465; 2017.11.21; see this OMIM report for additional information on specific gene associations.]

Cellular phenotype and pathology
Molecular information

Pharmacologic, neuroimaging, and animal-model findings suggest imbalances in monoaminergic (dopaminergic, serotonergic, and noradrenergic) neurotransmission in ADHD. [from MIM:143465; 2017.11.21]

Disease synonyms
ADHD
attention-deficit/hyperactivity disorder
attention deficit hyperactivity disorder
HKD
hyperactivity of childhood
hyperkinetic disorder
Ortholog Information
Human gene(s) in FlyBase
    Other mammalian ortholog(s) used
      D. melanogaster Gene Information (0)
      Other Genes Used: Viral, Bacterial, Synthetic (0)
        Summary of Physical Interactions (0 groups)
        Alleles Reported to Model Human Disease (Disease Ontology) (0 alleles)
        Alleles Representing Disease-Implicated Variants
        Genetic Tools, Stocks and Reagents
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        Contact lab of origin for a reagent not available from a public stock center.
        Bloomington Stock Center Disease Page
        Related mammalian, viral, bacterial, or synthetic transgenes
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        Selected Drosophila classical alleles
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        References (6)