Autosomal dominant hereditary disorder
Distal arthrogryposis syndrome
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Distal arthrogryposis type 1 (disorder)
Digitotalar dysmorphism
Distal arthrogryposis type 1
An autosomal dominant congenital anomaly characterized by contractures of the distal regions of the hands and feet with no facial involvement or any additional anomalies. It is the most common type of distal arthrogryposis.
distale artrogrypose type 1
DA1
Id715314008
StatusPrimitive
Associated morphologyContracture
Finding siteStructure of joint region
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationDecreased
InterpretsRange of joint movement
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ68.8
RuleTRUE
AdviceALWAYS Q68.8
CorrelationSNOMED CT source code to target map code correlation not specified