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Human Disease

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
Ontology
Human Disease   ( DOID:0111846 )
Relationships
is a type of
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Genes Involved
Zebrafish Models