Auditory perceptual disorders

disease
On this page

Also known as acoustic perceptual disorderacoustic perceptual disordersauditory comprehension disorderauditory comprehension disordersauditory inattentionauditory Inattentionsauditory perceptual disorderauditory processing disorderauditory processing disorderscomprehension disorder, auditorycomprehension disorders, auditorydisorder of sensory perception of sounddisorder, acoustic perceptualdisorder, auditory comprehensiondisorder, auditory processingdisorder, Psychoacousticaldisorders, acoustic perceptualdisorders, auditory comprehensiondisorders, auditory processingdisorders, Psychoacoustical

Summary

Auditory perceptual disorders (MONDO:0024422) is a disease and 19 clinical trials. A subtype of perceptual disorders — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 19

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameauditory perceptual disorders
Mondo IDMONDO:0024422
MeSHD001308
NCITC84575
SNOMED CT229752008
UMLSC0751257
MedGen155527
Is cancer (heuristic)no

Also known as: acoustic perceptual disorder · acoustic perceptual disorders · auditory comprehension disorder · auditory comprehension disorders · auditory inattention · auditory Inattentions · auditory perceptual disorder · auditory processing disorder · auditory processing disorders · comprehension disorder, auditory · comprehension disorders, auditory · disorder of sensory perception of sound · disorder, acoustic perceptual · disorder, auditory comprehension · disorder, auditory processing · disorder, Psychoacoustical · disorders, acoustic perceptual · disorders, auditory comprehension · disorders, auditory processing · disorders, Psychoacoustical (+11 more)

Disease family

This is a subtype of perceptual disorders. 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 body system or component › nervous system disorderperceptual disordersauditory perceptual disorders

Related subtypes (8): apraxia, vestibular disorder, agnosia, inherited retinal dystrophy, vision disorder, hearing disorder, allesthesia, hallucinogen-persisting perception disorder

Subtypes (1): hyperacusis

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: 19.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified19

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06117254Not specifiedRECRUITINGHearing Aids for Veterans With Functional Hearing Difficulties
NCT07039500Not specifiedRECRUITINGImpact of Severe Obstructive Sleep Apnea-Hypopnea Syndrome on Auditory-Cognitive Processing
NCT00004570Not specifiedTERMINATEDHereditary Deficits in Auditory Processing Leading to Language Impairment
NCT00167128Not specifiedUNKNOWNThe Phonak EduLink-System in Students With Specific Performance Deficits in Speech-in-Noise Intelligibility
NCT00264407Not specifiedCOMPLETEDNeural Changes in the Aging Auditory System
NCT01212068Not specifiedTERMINATEDConnectivity Analysis for Investigation of Auditory Impairment in Epilepsy
NCT02064257Not specifiedCOMPLETEDThe Listening Project: Tuning Into Change
NCT02353091Not specifiedCOMPLETEDEffects of Remote Microphone Hearing Aids on Children With Auditory Processing Disorder
NCT02398422Not specifiedCOMPLETEDThe Listening Project at Reiss-Davis/Vista Del Mar Child and Family Services
NCT02680730Not specifiedCOMPLETEDThe Listening Project at the ADD Centre and Biofeedback Institute of Toronto
NCT03468660Not specifiedCOMPLETEDAuditory Temporal Processes in Aging
NCT03475043Not specifiedCOMPLETEDNeuroplasticity in Auditory Aging_Project 2 Aims 1 and 2
NCT03648502Not specifiedTERMINATEDValidation of Cognitive Screenings for the Hearing Impaired
NCT03695575Not specifiedUNKNOWNAn ‘Off-the-shelf’ Assistive Listening Device: Normal-hearing Children.
NCT03887182Not specifiedCOMPLETEDContribution of Functional MRI in Assessment of Auditory Processing Disorders
NCT04363580Not specifiedTERMINATEDCreation of Auditory Processing Disorder Screening Tool in French
NCT04431622Not specifiedWITHDRAWNObjective Measurement of Hearing Aid Benefit
NCT05452486Not specifiedCOMPLETEDAuditory Processing in Spanish-English Bilinguals: Is Performance Better When Tested in Spanish or English?
NCT06970444Not specifiedCOMPLETEDtaVNS Effect on Central Auditory Processing

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.