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 1G ID (Ontology) DOID:0110834 (Human Disease)
Definition An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25.
Also Known As "USH1G" ; "Usher syndrome type IG"
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 Genes
 Usher syndrome type 1G       1
 for disease ribbon | Usher syndrome type 1G       1
 model of | Usher syndrome type 1G       1
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  Usher syndrome
   |__Usher syndrome type 1
       |__Usher syndrome type 1G  1 rec.
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Is a Usher syndrome type 1
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Synonyms
  • "USH1G" EXACT OMO:0003012
    "Usher syndrome type IG" EXACT
Secondary IDs
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ICD10CM:H35.5
MIM:606943