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:222800 - ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8

Xenbase Genes: bpgm

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009113 - hemolytic anemia due to diphosphoglycerate mutase deficiency

Disease Ontology (DO):
DOID:0111630 - familial erythrocytosis 8