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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](img/icons/info1.png)
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)