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Jacobsen syndrome

Disease Summary
Associated Targets (3)
Tbio

3


GARD Rare
Mondo Description Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.
Mondo Term and Equivalent IDs
MONDO:0007838:  Jacobsen syndrome
DOID:0111723: 
GARD:0000307: 
NCIT:C75457: 
Orphanet:2308: 
SCTID:715438008: 
UMLS:C0795841: