| Metadata | |
|---|---|
| ID | DOID:0060390 |
| Name | distal 10q deletion syndrome |
| Definition | A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10. https://rarediseases.info.nih.gov/diseases/3711/chromosome-10q-deletion |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
chromosome 10q26 deletion syndrome [EXACT] distal monosomy 10q [EXACT] monosomy 10qter [EXACT] telomeric deletion 10q [EXACT] terminal chromosome 10q26 deletion syndrome [EXACT] |
| Parent Relationships |