FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term otosclerosis 11 ID (Ontology) DOID:0060928 (Human Disease)
Definition An otosclerosis that is characterized by onset of progressive hearing loss in the second to third decade of life and that has_material_basis_in the locus associated with Forkhead Box L1 gene (FOXL1) on chromosome 16q24.
Also Known As "OTSC11"
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 Genes
 otosclerosis 11       4
 for disease ribbon | otosclerosis 11       4
 model of | otosclerosis 11       4
Spanning Tree (Parents/Children)
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autosomal dominant disease__
inner ear disease___________|
                            otosclerosis
                             |__otosclerosis 11  4 rec.
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Synonyms
  • "OTSC11" EXACT OMO:0003012
Secondary IDs
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MIM:620576