| Term Name: | chromosome 10q23 deletion syndrome | 
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| Synonyms: | |
| Definition: | A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2. | 
| Ontology: | Human Disease [DOID:0060389] ( DOID:0060389 ) |