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Metadata
ID DOID:0111363
Name Heinz body anemia
Definition A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in the HBA1, HBA2 or HBB genes on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively.
https://www.ncbi.nlm.nih.gov/pubmed/14184033, https://www.ncbi.nlm.nih.gov/pubmed/3997544, https://www.ncbi.nlm.nih.gov/pubmed/8704193
Xrefs

GARD:10718

MIM:140700

Subsets

DO_rare_slim

Parent Relationships

is_a congenital nonspherocytic hemolytic anemia

is_a autosomal dominant disease

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