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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 the SPTB gene on chromosome 14q23.3.

Synonyms: hereditary spherocytosis 2, HS2, SPH2

Xenbase Genes : sptb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000913 - interstitial fluid

MIM:
MIM:616649 - SPHEROCYTOSIS, TYPE 2; SPH2

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

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