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DOID:589 - congenital hemolytic anemia
Disease Ontology Definition:n_a
Synonyms: congenital hemolytic anaemia, hereditary hemolytic anaemia, hereditary hemolytic anemia,
Xenbase Genes : hba1, sptb, cdin1, gpi, g6pd, hba2, sec23b, atp11c, slc4a1, cdan1, cask, ank1, pklr, epb42
MONDO:0003689 - familial hemolytic anemia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hemolytic anemia (is_a),
physical disorder (is_a)