congenital nonspherocytic hemolytic anemia

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

Summary

Literature (0)

DOID:2861 - congenital nonspherocytic hemolytic anemia

Disease Ontology Definition:n_a

Synonyms: hereditary nonspherocytic hemolytic anemia, HNSHA, congenital nonspherocytic hemolytic anaemia, hereditary nonspherocytic hemolytic anaemia

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cask, pklr, g6pd

MIM:

MIM:300908 - anemia, nonspherocytic hemolytic, due to g6pd deficiency
MIM:613470 - hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency

MIM:300908 - anemia, nonspherocytic hemolytic, due to g6pd deficiency

MIM:613470 - hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): congenital hemolytic anemia (is_a)