Dyshematopoietic anemia congenital)
Anemia, congenital dyserythropoietic
A familial disorder characterized by anemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors erythroid precursor cells). Type ii is the most common of the 3 types; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test.
A rare congenital anemia caused by mutations in the cdan1 and sec23b genes.
D64.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM D64.4 became effective on October 1, 2022.
This is the American ICD-10-CM version of D64.4 – other international versions of ICD-10 D64.4 may differ.