Ring chromosome 22 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including global developmental delay, hypotonia, growth retardation with microcephaly, intellectual disability with severe speech delay, seizures or abnormal EEG, autistic spectrum disorder and other behavioral characteristics.

Synonyms: r(22) syndrome Ring 22 Ring chromosome 22

This is just here as a test because I lose it

Term information

database cross reference
expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=1446

hasDbXref

UMLS:C0265492

MeSH:C536795

ICD-10:Q93.2

UMLS:C2931325

has age of onset

http://www.orpha.net/ORDO/Orphanet_409945

http://www.orpha.net/ORDO/Orphanet_409944

has point prevalence range

http://www.orpha.net/ORDO/Orphanet_409979

notation

ORPHA:1446

part of

http://www.orpha.net/ORDO/Orphanet_363203

present in

http://www.orpha.net/ORDO/Orphanet_409991

Term relations

Subclass of: