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Echinobase
Summary Literature (0)
DOID:0110917 - hereditary spherocytosis type 2

Disease Ontology Definition:A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SPTB on chromosome 14q23.3.

Synonyms: HS2, SPH2, hereditary spherocytosis 2,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spherocytosis (is_a)