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trisomy 18

Disease Summary
Associated Targets (2)
Tclin

1

Tbio

1


GARD Rare
Mondo Description Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterized by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.
Mondo Term and Equivalent IDs
MONDO:0018071:  trisomy 18
GARD:0006321: 
ICD9:758.2: 
MESH:C580500: 
NCIT:C36626: 
Orphanet:3380: 
SCTID:51500006: 
UMLS:C0152096: