Term Name:	hereditary spherocytosis type 4
Synonyms:	hereditary spherocytosis 4, HS4, SPH4
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31.
Ontology:	Human Disease [DOID:0110919]   ( DOID:0110919 )