Disease

Congenital Hemolytic Anemia

About the Disease
Congenital Hemolytic Anemia, also known as anemia, hemolytic, congenital, is related to triosephosphate isomerase deficiency and congenital dyserythropoietic anemia. An important gene associated with Congenital Hemolytic Anemia is SPTA1 (Spectrin Alpha, Erythrocytic 1), and among its related pathways/superpathways are Clear cell renal cell carcinoma pathways and Interaction between L1 and Ankyrins. The drugs Benzocaine and Tannic acid have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, myeloid and bone, and related phenotypes are no effect and no effect

Common Targets
EPB41 | EPB42 | ADAMTS13 | GSS | RHAG | ALAS2 | GATA1 | SLC25A38 | RHD | ABCB6 | PKLR | SPTA1 | SLC4A1 | KCNN4 | ANK1 | PIEZO1 | G9429 | GCLC | ABCG5 | HBA1 | SPTB | CYB5R3 | ABCG8 | HK1 | GPI | SLC2A1 | BPGM | AK1 | TPI1 | CDAN1 | G6PD | GSTP1 | UGT1A1 | ALDOA

疾病靶点研报
Congenital Hemolytic Anemia

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