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DOID:1340 - pure red-cell aplasia
Disease Ontology Definition:A congenital hypoplastic anemia that is characterized by a normocytic normochromic anemia with severe reticulocytopenia and marked reduction or absence of erythroid precursors from the bone marrow.
Synonyms: primary red cell aplasia, pure red cell aplasia, Pure red cell aplasia, Pure Red cell Aplasia, Pure red cell aplasia (disorder), Red cell hypoplasia
Xenbase Genes
:
gata1,
rpl15,
rps26,
rpl26,
rps24,
rps19,
rps10,
rpl35,
rps7,
rps15a,
rpl5,
tsr2,
rpl27,
rpl11,
rpl18,
| MONDO:0001705 - pure red-cell aplasia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
aplastic anemia (is_a)