OBO ID: DOID:0110918 |
Term Name: | hereditary spherocytosis type 3 | Search Ontology: | |
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Synonyms: |
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Definition: | A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1. https://www.ncbi.nlm.nih.gov/pubmed/8941647 | ||
References: | |||
Ontology: | Human Disease ( DOID:0110918 ) |
OTHER hereditary spherocytosis type 3 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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SPTA1 | Spherocytosis, type 3 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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