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| Term | alpha thalassemia | ID (Ontology) | DOID:1099 (Human Disease) |
| Definition | A thalassemia involving the genes HBA1and HBA2 hemoglobin genes. | ||
| Also Known As | "Alpha thalassaemia" ; "alpha-Thalassemia" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ microcytic anemia____________| thalassemia |__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. |
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| Is a | thalassemia | ||
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GARD:621 ICD10CM:D56.0 ICD9CM:282.43 MESH:D017085 MIM:604131 NCI:C34368 SNOMEDCT_US_2023_03_01:191186002 UMLS_CUI:C0002312 |
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