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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/3997544, https://www.ncbi.nlm.nih.gov/pubmed/8704193, https://www.ncbi.nlm.nih.gov/pubmed/14184033
Xrefs	GARD:10718 MIM:140700
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant disease is_a congenital nonspherocytic hemolytic anemia
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance