X-linked congenital hemolytic anemia

Term ID

DOID:0111846

Synonyms

Definition

A congenital hemolytic anemia characterized by mild congenital hemolytic anemia without morphologic red cell abnormalities that has_material_basis_in hemizygous mutation in the ATP11C gene on chromosome Xq27.1. https://www.ncbi.nlm.nih.gov/pubmed/26944472

References

• OMIM:301015

Ontology

Human Disease   ( DOID:0111846 )