NIH GARD Information: Chromosome 17q11.2 deletion syndrome
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
Synonyms
- Chromosome 17q11.2 deletion syndrome, 1.4Mb
- VAN ASPEREN SYNDROME
- Monosomy 17q11
- NF1 microdeletion syndrome
- 17q11 microdeletion syndrome
- Del(17)(q11)
- Neurofibromatosis type 1 microdeletion syndrome
Overview
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.
