Autosomal dominant hereditary spastic paraplegia
Complicated hereditary spastic paraplegia
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Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)
Spastic paraplegia, neuropathy, poikiloderma syndrome
Antinolo Nieto Borrego syndrome
A complex form of hereditary spastic paraplegia with characteristics of spastic paraplegia, demyelinating peripheral sensorimotor neuropathy, poikiloderma (manifesting with loss of eyebrows and eyelashes in childhood in addition to delicate, smooth, and wasted skin) and distal amyotrophy (presenting after puberty). There have been no further descriptions in the literature since 1992.
syndroom van spastische paraplegie, neuropathie en poikilodermie
Id763402002
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
TargetG82.1
RuleTRUE
AdviceALWAYS G82.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG60.8
RuleTRUE
AdviceALWAYS G60.8
CorrelationSNOMED CT source code to target map code correlation not specified
TargetL81.8
RuleTRUE
AdviceALWAYS L81.8
CorrelationSNOMED CT source code to target map code correlation not specified