Term Name:	hereditary spherocytosis type 2
Synonyms:	hereditary spherocytosis 2, HS2, SPH2
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTB gene on chromosome 14q23.3.
Ontology:	Human Disease [DOID:0110917]   ( DOID:0110917 )