Term Name:	hereditary spherocytosis type 5
Synonyms:	hereditary spherocytosis 5, HS5, SPH5
Definition:	A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2.
Ontology:	Human Disease [DOID:0110920]   ( DOID:0110920 )