OBO ID: DOID:11198 |
Term Name: | DiGeorge syndrome | Search Ontology: | |
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Definition: | A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. (2) | ||
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Ontology: | Human Disease ( DOID:11198 ) |
OTHER DiGeorge syndrome PAGES
ZEBRAFISH MODELS
Fish | Conditions | Citations |
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tbx1tm208/tm208 | standard conditions | Piotrowski et al., 2003 |
PHENOTYPE
No data available
CITATIONS (4)
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