WormBase Tree Display for DO_term: DOID:0110918

DOID:0110918 Name: hereditary spherocytosis type 3
  Status: Valid
  Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1.
  Synonym: Exact: HS3
      SPH3
      hereditary spherocytosis 3
  Parent: Is_a: DOID:12971
      DOID:0050737
  DB_info: Database: OMIM disease 270970
  Attribute_of: Gene_by_orthology: WBGene00004951