Congenital hereditary muscular dystrophy
|
Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder)
Congenital muscular dystrophy with arthrogryposis multiplex congenita
congenitale spierdystrofie met arthrogryposis multiplex congenita
congenitale spierdystrofie met AMC
Id240061000
StatusPrimitive
Associated morphologyDystrophy
Finding siteSkeletal muscle structure
OccurrenceCongenital
Pathological processPathological developmental process
Clinical courseProgressive
ICD-10 complex map reference set
TargetG71.0
RuleTRUE
AdviceALWAYS G71.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ74.3
RuleTRUE
AdviceALWAYS Q74.3
CorrelationSNOMED CT source code to target map code correlation not specified