WormBase Tree Display for DO_term: DOID:0070116

DOID:0070116 Name: Meckel syndrome 2
  Status: Valid
  Definition: A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2.
  Synonym: Exact: MKS2
      Meckel-Gruber syndrome, type 2
  Parent: Is_a: DOID:0050778
  DB_info: Database: OMIM disease 603194
  Attribute_of: Gene_by_orthology: WBGene00194710