OBO ID: DOID:0050641 |
Term Name: | Rh deficiency syndrome | Search Ontology: | |
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Definition: | A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12. (2) | ||
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Ontology: | Human Disease ( DOID:0050641 ) |
OTHER Rh deficiency syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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