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NKX6-2-gerelateerde autosomaal recessieve hypomyeliniserende leukodystrofie (aandoening)
NKX6-2-gerelateerde autosomaal recessieve hypomyeliniserende leukodystrofie
SPAX 8
spastische ataxie type 8
NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy
Autosomal recessive hypomyelinating leukodystrophy, progressive spastic ataxia
SPAX8 - spastic ataxia 8
A rare leukodystrophy characterized by a spectrum of progressive neurologic manifestations comprising rapidly progressive early-onset nystagmus, spastic tetraplegia and visual and hearing impairment, resulting in death in early childhood, as well as later onset of slowly progressive complex spastic ataxia with pyramidal and cerebellar symptoms and loss of developmental milestones. Brain imaging shows diffuse hypomyelination of the subcortical and deep white matter, cerebellar atrophy and diffuse spinal cord volume loss.
Id1217379007
StatusPrimitive
Clinical courseprogressief
Has interpretationverlaagd
Interpretsgehoorfunctie
Has interpretationgestoord
InterpretsAdaptation behavior
Has interpretationgestoord
Interpretsintellectueel vermogen
Has interpretationafwezig
InterpretsMovement observable
InterpretsMovement
SNOMED CT to Orphanet simple map527497
SNOMED CT to ICD-10 extended map
TargetE75.2
RuleTRUE
AdviceALWAYS E75.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified