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congenital deafness
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MPZL2
ROR1
WBP2
ESRP1
EPS8L2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
sensory perception of mechanical stimulus
inner ear development
actin-based cell projection
ear morphogenesis
embryonic organ morphogenesis
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Curated Studies
Most Correlated Studies
OMIM - Choroideremia, deafness, and mental retardation
OMIM - Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome
OMIM - Multisystem Complex Disorders
OMIM - Developmental disorders
OMIM - Congenital deafness
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Literature
Most Relevant Literature
Genetics of congenital deafness].
Cystic cochleovestibular anomaly presenting with congenital deafness and recurrent bacterial meningi…
A case of palmoplantar lichen planus in a patient with congenital sensorineural deafness.
Congenital deafness in Jack Russell terriers: prevalence and association with phenotype.
Lateral superior olive function in congenital deafness.
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Clinical Trials
Most Relevant Clinical Trials
Degenerative Consequences of Congenital Deafness
Neuroanatomy of Reading in Congenital Deafness.
NGS Assessment of Congenitally Deafned Children and Neonatal Deafness Screnning
Evaluation of the Benefit of Antiviral Treatment With Valganciclovir on Congenital CMV Infection-rel…
Evaluation of a Cohort of Congenital Deep Deafness Patients and/or With Auditory Neuropathy, Looking…
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