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otosclerosis
(phenotype)
Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
FOXL1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
DESCARTES_MAIN_FETAL_MESANGIAL_CELLS
Fork head domain conserved site1
DESCARTES_FETAL_HEART_SMOOTH_MUSCLE_CELLS
Fork head domain conserved site 2
Fork head domain
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OMIM - Deafness and Ear Disorders
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Literature
Most Relevant Literature
Computed Tomography Density as a Bio-marker for Histologic Grade of Otosclerosis: A Human Temporal B…
Cellular voids in the pathogenesis of otosclerosis.
Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with o…
Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis.
A Systematic Review of the Effectiveness of Bisphosphonates for Otosclerosis.
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Clinical Trials
Most Relevant Clinical Trials
Study of Binaural Squelch Effect in Unilateral Otosclerosis
Cone Beam vs MDCT for Diagnosis and Pre-operative Evaluation of Otosclerosis
Hearing Aid Versus Surgical Rehabilitation as Treatment of Otosclerosis: Pilot Study
Cone Beam and CT Scan for the Diagnosis of Otosclerosis (TACOS)
Quantification of Prosthesis Penetration With Conebeam in Otosclerosis
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