|OBO ID: DOID:0060395|
|Term Name:||chromosome 15q24 deletion syndrome||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0060395)|
|is a type of:||
OTHER chromosome 15q24 deletion syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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