dystonia 12
human disease
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dystonia 12
Summary
dystonia 12 is a rare disease[1].
Key Facts
- dystonia 12's instance of is recorded as rare disease[2].
- dystonia 12's instance of is recorded as class of disease[3].
- dystonia 12 is a type of dystonia[4].
- dystonia 12 is a type of persistent combined dystonia[5].
- dystonia 12 is a type of rare genetic parkinsonian disorder[6].
- dystonia 12 is a type of genetic disease[7].
- dystonia 12 is a type of autosomal dominant disease[8].
- dystonia 12's NCI Thesaurus ID is recorded as C157577[9].
- dystonia 12's health specialty is recorded as neurology[10].
- dystonia 12's genetic association is recorded as ATP1A3[11].
- dystonia 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090056[12].
- dystonia 12's exact match is recorded as http://identifiers.org/doid/DOID:0090056[13].
- dystonia 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].