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

chromosome 17q23.1-q23.2 deletion syndrome

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description 17q23.1q23.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities.
Mondo Term and Equivalent IDs
MONDO:0013238:  chromosome 17q23.1-q23.2 deletion syndrome
GARD:0010936: 
Orphanet:261279: 
SCTID:719584008: 
UMLS:C3150607: 
UMLS:C4304591: