WormBase Tree Display for DO_term: DOID:0080255

DOID:0080255 Name: Meier-Gorlin syndrome 8
  Status: Valid
  Definition: A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12.
  Parent: Is_a: DOID:0050737
      DOID:0060306
  DB_info: Database: OMIM disease 617564
  Attribute_of: Gene_by_orthology: WBGene00003157