WormBase Tree Display for DO_term: DOID:0112160

DOID:0112160 Name: autosomal dominant nonsyndromic deafness 79
  Status: Valid
  Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22.
  Synonym: Exact: DFNA79
  Parent: Is_a: DOID:0050564
  DB_info: Database: OMIM disease 619086
  Attribute_of: Gene_by_orthology: WBGene00001397
      WBGene00001398
      WBGene00001399