Term Name:	hereditary spherocytosis type 3
Synonyms:	hereditary spherocytosis 3, HS3, SPH3
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1.
Ontology:	Human Disease [DOID:0110918]   ( DOID:0110918 )