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hypoacusis
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
SPTBN4
BCS1L
HPPD
CIHL
ARHI1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
sensory perception of mechanical stimulus
inner ear development
embryonic organ morphogenesis
ATPase, AAA-type, conserved site
ATPase, AAA-type, core
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Curated Studies
Most Correlated Studies
Inferior colliculus tissue from presbycusic middle-aged mice
Novel approach to select genes using functional hearing
Skin from GRHL2 mutant patients with ectodermal dysplasia and hearing loss
Cochlear tissues from CMAH knockout mice
OMIM - Deafness, dystonia, and cerebral hypomyelination
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Literature
Most Relevant Literature
Rare Gene Mutations in Romanian Hypoacusis Patients: Case Series and a Review of the Literature.
Sudden hearing loss after dental treatment.
c-Ret-mediated hearing losses.
Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss …
Teprotumumab and hearing loss: hear the warnings.
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Clinical Trials
Most Relevant Clinical Trials
AUditive Direct In-utero Observation (AUDIO): Prenatal Testing of Congenital Hypoacusis
Study of Binaural Squelch Effect in Unilateral Otosclerosis
Efficacy of AerosalĀ® in the Treatment of Sub-Obstructive Adenotonsillar Hypertrophy and Related Dise…
Effectiveness of a Program Based on Observation-action Training (AOT) in Patients With Cognitive Imp…
Musical Intervention in Non-invasive Ventilation
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