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
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| Id | 725433003 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G11.2 | Rule | TRUE | Advice | ALWAYS G11.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
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