WormBase Tree Display for DO_term: DOID:0080512

DOID:0080512 Name: Meier-Gorlin syndrome 1
  Status: Valid
  Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32.
  Parent: Is_a: DOID:0050737
      DOID:0060306
  DB_info: Database: OMIM disease 224690
  Attribute_of: Gene_by_orthology: WBGene00012650