OBO ID: DOID:0060395 |
Term Name: | chromosome 15q24 deletion syndrome | Search Ontology: | |
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Definition: | A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15. https://www.omim.org/entry/613406 | ||
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Ontology: | Human Disease ( DOID:0060395 ) |
OTHER chromosome 15q24 deletion syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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