OBO ID: DOID:0110919 |
Term Name: | hereditary spherocytosis type 4 | Search Ontology: | |
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Definition: | A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31. https://www.ncbi.nlm.nih.gov/pubmed/7530501 | ||
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Ontology: | Human Disease ( DOID:0110919 ) |
OTHER hereditary spherocytosis type 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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