ICD-11 code : 8A03.10;
Preferred Label : Friedreich ataxia;
ICD-11 definition : Friedreich ataxia is an autosomal recessive ataxia characterised by difficulties to
coordinate movements, associated with neurological signs (dysarthria, loss of reflexes,
decrease of deep sensation, pes cavus and scoliosis), cardiomyopathy and sometimes
diabetes mellitus. It is due to a mutation in the frataxin gene.;
Origin ID : 980686666;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- ICD-10 Mapping
- Validated automatic mappings to BTNT
Friedreich ataxia is an autosomal recessive ataxia characterised by difficulties to
coordinate movements, associated with neurological signs (dysarthria, loss of reflexes,
decrease of deep sensation, pes cavus and scoliosis), cardiomyopathy and sometimes
diabetes mellitus. It is due to a mutation in the frataxin gene.
