WormBase Tree Display for DO_term: DOID:0110832

DOID:0110832 Name: Usher syndrome type 1F
  Status: Valid
  Definition: An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q.
  Synonym: Exact: USH1F
      Usher syndrome type IF
  Parent: Is_a: DOID:0110826
  DB_info: Database: OMIM disease 602083
  Attribute_of: Gene_by_orthology: WBGene00000397