OBO ID: DOID:0111846 |
Term Name: | X-linked congenital hemolytic anemia | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0111846 ) |
OTHER X-linked congenital hemolytic anemia PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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