|||||
Xp22.13p22.2 duplication syndrome (disorder)
Xp22.13p22.2 duplication syndrome
A rare syndromic intellectual disability characterized by developmental delay and intellectual disability, learning and behavioral problems, short stature, thin and sparse hair, mild dysmorphic features, tapering fingers and later onset of scoliosis, obesity and cardiovascular problems (cardiomegaly and cardiomyopathy). Females have normal intelligence.
xp22.13p22.2-duplicatiesyndroom
Id782877002
StatusPrimitive
Associated morphologyPartial trisomy
Finding siteShort arm of chromosome
OccurrenceCongenital
Associated morphologyPartial trisomy
Finding siteSex chromosome X
OccurrenceCongenital
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ99.8
RuleTRUE
AdviceALWAYS Q99.8
CorrelationSNOMED CT source code to target map code correlation not specified