Autosomal dominant hereditary spastic paraplegia
Complicated hereditary spastic paraplegia
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Autosomal dominant spastic paraplegia type 36 (disorder)
Autosomal dominant spastic paraplegia type 36
A complex form of hereditary spastic paraplegia, with onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait, spasticity, lower limb weakness, pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy. The SPG36 phenotype has been mapped to a locus on chromosome 12q23-q24.
autosomaal dominante spastische paraplegie type 36
SPG36
Id723819007
StatusPrimitive
Associated morphologyDegenerative abnormality
Finding siteSpinal cord structure
Finding siteLower limb 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