hemolytic anemia

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Summary

Literature (0)

DOID:583 - hemolytic anemia

Disease Ontology Definition:A normocytic anemia that is characterized by the rate of descruction of red blood cells exceeding the rate than they can be made.

Synonyms: ANEMIA HEMOLYTIC

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

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

MIM:

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: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): normocytic anemia (is_a)