The association between PKM (Pyruvate Kinase M1/2) and Anemia, Congenital, Nonspherocytic Hemolytic, 2 is reported, with clinical genetic testing available.
Sources1
Clinical variants0
Symptoms38
Compounds1
Trials7of 28 via PKM compounds
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.