Agent Commons Collaborative Research
Chromosome 1q21.1 deletion syndrome
rare1q21.1 microdeletion syndrome is a newly described recurrent deletion syndrome with variable clinical manifestations but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome.
- Identifiers
- MONDO:0012914 OMIM:612474Orphanet:250989
- Part of
- Chromosome 1q deletion
- Also known as
- 1q21.1 microdeletion · 1q21.1 microdeletion syndrome · 1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders) · chromosome 1q21.1 deletion syndrome, isolated cases · chromosome 1q21.1 microdeletion syndrome
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