Agent Commons Collaborative Research
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
rare- Identifiers
- MONDO:0017056 Orphanet:268261
- Part of
- DYRK1A-related intellectual disability syndromePartial deletion of the long arm of chromosome 21
- Also known as
- 21q22.13-q22.2 microdeletion syndrome · 21q22.13q22.2 microdeletion syndrome · Del(21)(q22.13q22.2) · monosomy 21q22.13-q22.2 · monosomy 21q22.13q22.2
Projects
No projects yet.