FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Usher syndrome type 1B ID (Ontology) DOID:0070655 (Human Disease)
Definition An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the MYO7A gene on chromosome 11q13.
Also Known As "USH1B" ; "Usher syndrome type IB"
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 Genes
 Usher syndrome type 1B       1
 for disease ribbon | Usher syndrome type 1B       1
 model of | Usher syndrome type 1B       1
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  Usher syndrome
   |__Usher syndrome type 1
       |__Usher syndrome type 1B  1 rec.
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Is a Usher syndrome type 1
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Synonyms
  • "USH1B" EXACT OMO:0003012
    "Usher syndrome type IB" EXACT
Secondary IDs
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MESH:C536485
MIM:276900
UMLS_CUI:C2931206