You are using an outdated browser. Please upgrade your browser to improve your experience.

chromosome 2q32-q33 deletion syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description 2q32q33 microdeletion syndrome is a recently described syndrome characterized by a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.
Mondo Term and Equivalent IDs
MONDO:0012864:  chromosome 2q32-q33 deletion syndrome
GARD:0013206: 
MESH:C567350: 
Orphanet:251019: 
SCTID:719659003: 
UMLS:C2676739: 
UMLS:C4304531: