Congenital Hypoplastic Anemia

Overview of Congenital Hypoplastic Anemia

Most recent studies have shown that Congenital Hypoplastic Anemia shares some biological mechanisms with anemia, anemia-diamond-blackfan, anemia-hemolytic-congenital, aplasia-nos, aplastic-anemia, congenital-abnormality, congenital-anemia, cytogenetic-abnormality, decreased-erythroid-precursor-production, fanconi-anemia, fanconi-syndrome, hemosiderosis, hypoplasia, hypoplastic-anemia, leukemia, normocytic-anemia, pancytopenia, pure-red-cell-aplasia, transient-erythroblastopenia-of-childhood.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Hypoplastic Anemia, and have been seen in publications frequently: Cellular Localization, Chemotaxis, Excretion, Hemopoiesis, Localization, Macrophage Differentiation, Neutrophil Chemotaxis, Pathogenesis, Respiratory Burst, Response To Erythropoietin, Secretion, Translation

Quite a number of genes have been found to play important roles in Congenital Hypoplastic Anemia, such as ADA, CCDC6, CD34, ENO1, EPO, EPX, GPI, GZMM, KIT, NR4A3, PTCH1, RET, RPS19, TAS2R38, TCFL5, TCN2, TIMP1, UMPS. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Congenital Hypoplastic Anemia Related Genes

click to see detail information for each gene

Pathways Related to Congenital Hypoplastic Anemia

This information is being compiled and will come in a future update

Related Diseases