hemolytic anemia

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Echinobase

Summary

Literature (0)

DOID:583 - hemolytic anemia

Disease Ontology Definition:n_a

Synonyms: ANEMIA HEMOLYTIC,

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

: atrx, cask, cdin1, cdan1, pklr, g6pd, pigt

OMIM:

MIM:266120 - uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
MIM:612631 - adenylate kinase deficiency, hemolytic anemia due to

MIM:266120 - uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to

MIM:612631 - adenylate kinase deficiency, hemolytic anemia due to

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

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

Parent(s): normocytic anemia (is_a)