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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Autosomal genetic disease/ Autosomal recessive disease/ Autosomal recessive cerebellar ataxia/ Autosomal recessive syndromic cerebellar ataxia

Gemignani syndrome

rare

Identifiers: MONDO:0016159 Orphanet:2074
Part of: Autosomal recessive syndromic cerebellar ataxia
Also known as: spinocerebellar ataxia associated amyotrophy of the hands and sensorineural deafness · spinocerebellar ataxia-amyotrophy-deafness syndrome

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