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trisomy 13

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Explore Associated Targets
Mondo Description Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.
Mondo Term and Equivalent IDs
MONDO:0018068:  trisomy 13
GARD:0007341: 
ICD9:758.1: 
MESH:C536305: 
NCIT:C36529: 
Orphanet:3378: 
SCTID:21111006: 
UMLS:C0152095: 
UMLS:CN204386: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)