| autosomaal recessieve cerebellaire ataxie type 1 (aandoening) | | autosomaal recessieve cerebellaire ataxie type 1 | | autosomaal recessieve cerebellaire ataxie type Beauce
ARCA1
| | 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. |
| | Id | 725433003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G11.2 | | Term | Laat optredende cerebellaire ataxie |
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| SNOMED CT to Orphanet simple map | 88644 |
| SNOMED CT to ICD-10 extended map | | 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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