Spinocerebellar ataxia type 37 (disorder) | | Spinocerebellar ataxia type 37 | | Spinocerebellar ataxia with altered vertical eye movement
| | Disease with characteristics of cerebellar syndrome along with altered vertical eye movements. Reported in nine members of Spanish kindred to date. Disease onset occurs in adulthood (from the ages of 38-64). Clinical manifestations are slowly progressive cerebellar ataxia (starting with falls, dysarthria and clumsiness followed by other cerebellar signs) along with altered vertical eye movements. The causal gene is unknown but it has been mapped to chromosome 1p32 and named the SCA37 locus. Inherited in an autosomal dominant manner. | | spinocerebellaire ataxie type 37 | | SCA37
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| Id | 719301002 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G11.8 | Rule | TRUE | Advice | ALWAYS G11.8 | Correlation | SNOMED CT source code to target map code correlation not specified |
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