WormBase Tree Display for DO_term: DOID:0070128

DOID:0070128 Name: congenital nongoitrous hypothyroidism 6
  Status: Valid
  Definition: A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.
  Synonym: Exact: CHNG6
  Parent: Is_a: DOID:0050328
      DOID:0050736
  DB_info: Database: OMIM disease 614450
  Attribute_of: Gene_by_orthology: WBGene00003601