WormBase Tree Display for DO_term: DOID:0111448

DOID:0111448 Name: progressive myoclonus epilepsy 1B
  Status: Valid
  Definition: An Unverricht-Lundborg syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PRICKLE1 gene on chromosome 12q12.
  Synonym: Exact: EPM1B
  Parent: Is_a: DOID:3535
      DOID:0050737
  DB_info: Database: OMIM disease 612437
  Attribute_of: Gene_by_orthology: WBGene00022727