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| Term | thalassemia | ID (Ontology) | DOID:10241 (Human Disease) |
| Definition | A microcytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains. | ||
| Also Known As | "Sickle-cell thalassemia with crisis" ; "Sickle-cell thalassemia without crisis" ; "thalassemia Hb-S disease with crisis" (for all, see Synonyms field below) | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ anemia | |__microcytic anemia____________| thalassemia 3 rec. |__alpha thalassemia 3 rec. | |__alpha thalassemia-intellectual disability syndrome type 1 | |__alpha thalassemia-X-linked intellectual disability syndrome 2 rec. | |__hemoglobin H disease 1 rec. |__beta thalassemia 1 rec. |__autosomal dominant beta thalassemia 1 rec. |__beta-thalassemia intermedia |__beta-thalassemia major |__delta beta-thalassemia |__thalassemia minor |
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| Is a |
autosomal recessive disease microcytic anemia |
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External Crossreferences & Linkouts
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GARD:7756 ICD10CM:D56 ICD9CM:282.4 MESH:D013789 NCI:C35069 SNOMEDCT_US_2023_03_01:191192008 UMLS_CUI:C0039730 |
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