Autosomal dominant hereditary disorder
Omodysplasia
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Autosomal dominant omodysplasia (disorder)
Autosomal dominant omodysplasia
Omodysplasia 2
An autosomal dominant form of omodysplasia a rare skeletal dysplasia, in which stature is normal and shortening is limited to the upper limbs.
autosomaal dominante 'omodysplasia'
Id725165009
StatusPrimitive
Associated morphologyDysplasia
Finding siteBone structure
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetQ78.8
RuleTRUE
AdviceALWAYS Q78.8
CorrelationSNOMED CT source code to target map code correlation not specified