Autosomal dominant hereditary spastic paraplegia
Pure hereditary spastic paraplegia
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Autosomal dominant spastic paraplegia type 41 (disorder)
Autosomal dominant spastic paraplegia type 41
A pure form of hereditary spastic paraplegia with onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise.
autosomaal dominante spastische paraplegie type 41
SPG41
Id763069002
StatusPrimitive
Finding siteLower limb structure
Associated morphologyDegenerative abnormality
Finding siteSpinal cord structure
Clinical courseProgressive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG11.4
RuleTRUE
AdviceALWAYS G11.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified