Reading disorder

disease
On this page

Summary

Reading disorder (MONDO:0001697) is a disease and 7 clinical trials. Top therapeutic interventions include atomoxetine hydrochloride. A subtype of learning disability — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 7

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namereading disorder
Mondo IDMONDO:0001697
DOIDDOID:13365
SNOMED CT52824009
Is cancer (heuristic)no

Disease family

This is a subtype of learning disability. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by developmental or physiological process › psychiatric disordermental disorderdevelopmental disorder of mental healthspecific developmental disorderlearning disabilityreading disorder

Related subtypes (2): writing disorder, dyscalculia

Subtypes (3): alexia, dyslexia, hyperlexia

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified5
PHASE42

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00191906PHASE4COMPLETEDComparison of Atomoxetine and Placebo in Children With Attention-Deficit/Hyperactivity Disorder (ADHD) and/or Reading Disorder (RD)
NCT05854082PHASE4COMPLETEDImpact of Motor Tasks and Lidocaine on Reading Unfamiliar Words in Adults With and Without Dyslexia
NCT06213272Not specifiedRECRUITINGCombined Exercise and Targeted Therapy for Post-Stroke Reading Deficits
NCT02107534Not specifiedUNKNOWNGroup-based Training for Parents of Children With Dyslexia
NCT04113707Not specifiedWITHDRAWNBuilding Long-term Academic Success Through Ongoing Fun Fitness Program
NCT05137353Not specifiedCOMPLETEDA Multisensory Music Intervention for Children With Reading Disorders (RitMoZ)
NCT06186882Not specifiedUNKNOWNGene x Environment Interplay in Developmental Dyslexia Treatment: A Round-trip Translation Between Humans and Animal

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
ATOMOXETINE HYDROCHLORIDE41