congenital nonspherocytic hemolytic anemia

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Echinobase

Summary

Literature (0)

DOID:2861 - congenital nonspherocytic hemolytic anemia

Disease Ontology Definition:n_a

Synonyms: HNSHA, hereditary nonspherocytic hemolytic anemia,

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

: cask, pklr, g6pd

OMIM:

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): congenital hemolytic anemia (is_a)