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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00228 | Thalassemia | Thalassemia is the most common hereditary blood disease caused by mutation of genes encoding hemoglobin alpha and beta chains. The anemia that is associated with thalassemia is caused by ineffective erythropoiesis ... | Hematologic disease |
(Alpha) HBA1 [HSA:3039] [KO:K13822] (Alpha) HBA2 [HSA:3040] [KO:K13822] (Beta) HBB [HSA:3043] [KO:K13823] (Beta) HBG1 [HSA:3047] [KO:K13824] (Beta) HBG2 [HSA:3048] [KO:K13824] (ATRX) ATRX [HSA:546] [KO:K10779] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |