myoclonic dystonia 26
human disease
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Summary
myoclonic dystonia 26 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- myoclonic dystonia 26's instance of is recorded as rare disease[3].
- myoclonic dystonia 26's instance of is recorded as class of disease[4].
- myoclonic dystonia 26 is a type of myoclonic dystonia[5].
- myoclonic dystonia 26 is a type of genetic disease[6].
- myoclonic dystonia 26 is a type of autosomal dominant disease[7].
- myoclonic dystonia 26's genetic association is recorded as KCTD17[8].
- myoclonic dystonia 26's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090036[9].
- myoclonic dystonia 26's exact match is recorded as http://identifiers.org/doid/DOID:0090036[10].
- myoclonic dystonia 26's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
myoclonic dystonia 26 is known by 5 alternative names across languages and contexts.[2]