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chromosome 1q41-q42 deletion syndrome

Disease Summary
Associated Targets (3)
Tbio

3


GARD Rare
Mondo Description 1q41q42 microdeletion syndrome is a chromosomal anomaly characterized by a severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
Mondo Term and Equivalent IDs
MONDO:0012927:  chromosome 1q41-q42 deletion syndrome
GARD:0003738: 
Orphanet:250999: 
SCTID:716515000: 
UMLS:C2675857: 
UMLS:C4274528: