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Summary Literature (0)
DOID:10241 - thalassemia

Disease Ontology Definition:A microcytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains.

Synonyms: Sickle-cell thalassemia with crisis, Sickle-cell thalassemia without crisis, thalassemia Hb-S disease with crisis, thalassemia Hb-S disease without crisis

Xenbase Genes : hba1, hba2, atrx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000984 - porous


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), hemolytic anemia (is_a), microcytic anemia (is_a)