autosomaal dominante hereditaire aandoening
spinocerebellaire ataxie
|
|
spinocerebellaire ataxie type 35 (aandoening)
spinocerebellaire ataxie type 35
SCA35
Spinocerebellar ataxia type 35
An autosomal dominant cerebellar ataxia type 1 that is characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor of hands, hyperreflexia and spasmodic torticollis.
Id
719300001
Status
Primitive
Associated morphology
degeneratieve afwijking
Finding site
structuur van cerebellum
Associated morphology
degeneratieve afwijking
Finding site
structuur van medulla spinalis
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map
276193
SNOMED CT to ICD-10 extended map
Target
G11.8
Rule
TRUE
Advice
ALWAYS G11.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation
SNOMED CT source code to target map code correlation not specified