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bn:00054147n
Noun Concept
Categories: Disorders of globin and globulin proteins, Articles with permanently dead external links, Hereditary hemolytic anemias, Mediterranean, Autosomal recessive disorders
EN
thalassemia  thalassaemia  Mediterranean anemia  Mediterranean anaemia
EN
An inherited form of anemia caused by faulty synthesis of hemoglobin WordNet 3.0
Definitions
Relations
Sources
EN
An inherited form of anemia caused by faulty synthesis of hemoglobin WordNet 3.0 & Open English WordNet
Thalassemias are inherited blood disorders that result in abnormal hemoglobin. Wikipedia
Human disease Wikidata
Any of a group of inherited disorders in which the amount of hemoglobin in the blood is reduced. Wiktionary
IS A
hypochromic anemia
monogenic disorder
hemoglobinopathy
hemolytic anemia
autosomal recessive disease
HAS KIND
Cooley's anemia
hemoglobin Barts
delta-beta thalassemia
alpha-thalassemia
beta thalassemia
DRUG USED FOR TREATMENT
deferoxamine
deferasirox
deferiprone
HEALTH SPECIALTY
hematology
WordNet 3.0 & Open English WordNet
EN
thalassemia, thalassaemia, Mediterranean anemia, Mediterranean anaemia
Wikipedia
EN
thalassemia
Wikidata
EN
thalassemia
Wiktionary
EN
thalassemia
Wikipedia Redirections
EN
Alpha Thalassaemia, Erythroblastic Anemia, Erythroblastic anemia, Gene therapy for thalassemia, hemoglobin H, Mediterranean anemia, Thalasaemia, Thalasemia, thalassaemia, thalassaemia intermedia, Thalassaemia Minor, Thalassaemia minor, thalassaemias, thalassemias, Thalesemia, thalessemia, Thallasemia, Thallassemia, Thallesemia, Thallessemia
Wikidata Alias
EN
Sickle-cell thalassemia with crisis, Sickle-cell thalassemia without crisis, thalassemia Hb-S disease with crisis, thalassemia Hb-S disease without crisis

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