congenital nonspherocytic hemolytic anemia 1

Term ID

DOID:0051003

Synonyms

Definition

A congenital nonspherocytic hemolytic anemia that has_material_basis_in mutation in the G6PD gene on chromosome Xq28, and is the most common genetic form of chronic and drug-, food-, or infection-induced hemolytic anemia. https://pubmed.ncbi.nlm.nih.gov/18177777/

References

• MIM:300908

Ontology

Human Disease   ( DOID:0051003 )