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What is another word for autosomal dominant cerebellar ataxia?

Pronunciation: [ˌɔːtə͡ʊsˈə͡ʊmə͡l dˈɒmɪnənt sˈɛɹɪbˌɛləɹ atˈe͡ɪksi͡ə] (IPA)

Autosomal dominant cerebellar ataxia is a genetic disorder that affects the cerebellum, causing problems with movement, balance, speech, and coordination. There are several other terms used to describe this condition, including spinocerebellar ataxia, hereditary ataxia, and dominant ataxia. Many different types of autosomal dominant cerebellar ataxia exist, each caused by a different mutation in a specific gene. Some examples include spinocerebellar ataxia type 1, spinocerebellar ataxia type 2, and spinocerebellar ataxia type 6. Despite the different names used to describe this disorder, they refer to the same underlying condition.
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Synonyms for Autosomal dominant cerebellar ataxia:

What are the hypernyms for Autosomal dominant cerebellar ataxia?

A hypernym is a word with a broad meaning that encompasses more specific words called hyponyms.

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autosomal dominant cerebellar ataxia, synonym autosomal dominant cerebellar ataxia, another word for autosomal dominant cerebellar ataxia, words like autosomal dominant cerebellar ataxia, thesaurus autosomal dominant cerebellar ataxia
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