WormBase Tree Display for DO_term: DOID:0112168

DOID:0112168 Name: autosomal dominant nonsyndromic deafness 77
  Status: Valid
  Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11.
  Synonym: Exact: DFNA77
  Parent: Is_a: DOID:0050564
  DB_info: Database: OMIM disease 618915
  Attribute_of: Gene_by_orthology: WBGene00003407
      WBGene00003408
      WBGene00003413