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complete deafness
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
HPPD
SDHD
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
sensory perception of mechanical stimulus
inner ear morphogenesis
Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS
ear morphogenesis
Fumarate reductase/succinate dehydrogenase, transmembrane subunit
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Curated Studies
Most Correlated Studies
OMIM - Hypertelorism
Cancer Gene Census - mutations in cancer genes
OMIM - Cancer
Mouse Phenotypes - Disorder of head
Lymphoblastoid lines of family with maternally inherited non-syndromic hearing loss
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Literature
Most Relevant Literature
Cell-type-specific roles of Na+/K+ ATPase subunits in Drosophila auditory mechanosensation.
Chemotherapy: present and future.
Surgical treatment of adult cholesteatoma: long-term follow-up using total reconstruction procedure …
Intralabyrinthine schwannoma extending into the round window niche and internal auditory canal].
Preservation of auditory P300-like potentials in cortical deafness.
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Clinical Trials
Most Relevant Clinical Trials
Genetic Studies of Tone Deafness
Efficacy of the Bone-anchored Hearing Aid for Unilateral Deafness
Single-sided Deafness and Cochlear Implantation
Development of a Deaf Child With a Cochlear Implant.
Outcomes In Children With Developmental Delay And Deafness
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