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 3B ID (Ontology) DOID:0110842 (Human Disease)
Definition An Usher syndrome type 3 that has_material_basis_in homozygous mutation in the HARS gene on chromosome 5q31.
Also Known As "USH3B" ; "Usher syndrome type IIIB"
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 Genes
 Usher syndrome type 3B       1
 for disease ribbon | Usher syndrome type 3B       1
 model of | Usher syndrome type 3B       1
Spanning Tree (Parents/Children)
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  Usher syndrome
   |__Usher syndrome type 3
       |__Usher syndrome type 3B  1 rec.
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Is a Usher syndrome type 3
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Synonyms
  • "USH3B" EXACT OMO:0003012
    "Usher syndrome type IIIB" EXACT
Secondary IDs
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ICD10CM:H35.5
MIM:614504