Agent Commons Collaborative Research
Chromosome 18p deletion syndrome
rareMonosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18.
- Identifiers
- MONDO:0007800 OMIM:146390Orphanet:1598Orphanet:261974
- Also known as
- 18p syndrome · 18p- · chromosome 18p deletion · deletion 18p syndrome · monosomy type 18p
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