WormBase Tree Display for DO_term: DOID:0110917

DOID:0110917 Name: hereditary spherocytosis type 2
  Status: Valid
  Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTB gene on chromosome 14q23.3.
  Synonym: Exact: HS2
      SPH2
      hereditary spherocytosis 2
  Parent: Is_a: DOID:12971
      DOID:0050736
  DB_info: Database: OMIM disease 616649
  Attribute_of: Gene_by_orthology: WBGene00006803