| Term Name: | chromosome 10q23 deletion syndrome |
|---|---|
| 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 ) |