Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:616649 - SPHEROCYTOSIS, TYPE 2; SPH2

Xenbase Genes: sptb

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000913 - interstitial fluid
MONDO:0019350 - hereditary spherocytosis

Disease Ontology (DO):
DOID:0110917 - hereditary spherocytosis type 2