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Autosomal recessive cerebellar ataxia Beauce type (disorder)
Autosomal recessive cerebellar ataxia Beauce type
ARCA1 - autosomal recessive cerebellar ataxia type 1
Disease with characteristics of slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations.
autosomaal recessieve cerebellaire ataxie type 1
ARCA1
autosomaal recessieve cerebellaire ataxie type Beauce
Id725433003
StatusPrimitive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG11.2
RuleTRUE
AdviceALWAYS G11.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified