WormBase Tree Display for DO_term: DOID:0112187

DOID:0112187 Name: thyroid dyshormonogenesis 3
  Status: Valid
  Definition: A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TG on chromosome 8q24.22.
  Synonym: Exact: TDH3
      genetic defect in thyroid hormonogenesis 3
  Parent: Is_a: DOID:0050737
      DOID:0112183
  DB_info: Database: OMIM disease 274700