Congenital hereditary muscular dystrophy
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Merosin deficient congenital muscular dystrophy (disorder)
Merosin deficient congenital muscular dystrophy
merosinedeficiënte congenitale spierdystrofie
laminine-alfa2-deficiënte congenitale spierdystrofie
Id111503008
StatusPrimitive
Associated morphologyDystrophy
Finding siteSkeletal muscle structure
OccurrenceCongenital
Pathological processPathological developmental process
Clinical courseProgressive
Dutch rare neuromuscular disorders simple reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG71.2
RuleTRUE
AdviceALWAYS G71.2
CorrelationSNOMED CT source code to target map code correlation not specified