WormBase Tree Display for DO_term: DOID:0070013

DOID:0070013 Name: Seckel syndrome 2
  Status: Valid
  Definition: A Seckel syndrome that has_material_basis_in homozygous mutation in the RBBP8 gene on chromosome 18q11.
  Synonym: Exact: SCKL2
      Seckel-type dwarfism 2
      microcephalic primordial dwarfism 2
  Parent: Is_a: DOID:0050569
  DB_info: Database: OMIM disease 606744
  Attribute_of: Gene_by_orthology: WBGene00008082