WormBase Tree Display for DO_term: DOID:0110831

DOID:0110831 Name: Usher syndrome type 1D
  Status: Valid
  Definition: An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
  Synonym: Exact: USH1D
      Usher syndrome type ID
  Parent: Is_a: DOID:0080578
      DOID:0110826
  DB_info: Database: OMIM disease 601067
  Attribute_of: Gene_by_orthology: WBGene00000397