Term Name:	hereditary spherocytosis type 1
Synonyms:	hereditary spherocytosis 1, HS1, SPH1
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the ANK1 gene on chromosome 8p11.21.
Ontology:	Human Disease [DOID:0110916]   ( DOID:0110916 )