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chromosome 18p deletion syndrome

Disease Summary
Associated Targets (0)

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Mondo Description Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18.
Mondo Term and Equivalent IDs
MONDO:0007800:  chromosome 18p deletion syndrome
GARD:0008631: 
MESH:C538309: 
NCIT:C84521: 
Orphanet:1598: 
SCTID:270890001: 
UMLS:C0432442: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found