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| Term | congenital dyserythropoietic anemia | ID (Ontology) | DOID:1338 (Human Disease) |
| Definition | A congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood. | ||
| Also Known As | "congenital dyshaematopoietic anaemia" | ||
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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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physical disorder__ hemolytic anemia___| congenital hemolytic anemia |__congenital dyserythropoietic anemia 8 rec. |__congenital dyserythropoietic anemia type I 2 rec. | |__congenital dyserythropoietic anemia type Ia 1 rec. | |__congenital dyserythropoietic anemia type Ib 1 rec. |__congenital dyserythropoietic anemia type II 1 rec. |__congenital dyserythropoietic anemia type IIIa 1 rec. |__congenital dyserythropoietic anemia type IIIb 2 rec. |__congenital dyserythropoietic anemia type IVa 2 rec. |__congenital dyserythropoietic anemia type IVb 2 rec. |
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| Is a | congenital hemolytic anemia | ||
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GARD:1999 ICD10CM:D64.4 MESH:D000742 MIM:PS224120 NCI:C84646 ORDO:85 SNOMEDCT_US_2023_03_01:191272005 UMLS_CUI:C0002876 |
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