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's subclass of is recorded as dystonia[4].
- dystonia 12's subclass of is recorded as persistent combined dystonia[5].
- dystonia 12's subclass of is recorded as rare genetic parkinsonian disorder[6].
- dystonia 12's subclass of is recorded as genetic disease[7].
- dystonia 12's subclass of is recorded as autosomal dominant disease[8].
- dystonia 12's OMIM ID is recorded as 128235[9].
- dystonia 12's Disease Ontology ID is recorded as DOID:0090056[10].
- dystonia 12's Orphanet ID is recorded as 71517[11].
- dystonia 12's NCI Thesaurus ID is recorded as C157577[12].
- dystonia 12's health specialty is recorded as neurology[13].
- dystonia 12's genetic association is recorded as ATP1A3[14].
- dystonia 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090056[15].
- dystonia 12's exact match is recorded as http://identifiers.org/doid/DOID:0090056[16].
- dystonia 12's UMLS CUI is recorded as C1868681[17].
- dystonia 12's ICD-10-CM is recorded as G24.1[18].
- dystonia 12's GARD rare disease ID is recorded as 9628[19].
- dystonia 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- dystonia 12's Mondo ID is recorded as MONDO_0007496[21].
- dystonia 12's Genetics Home Reference Conditions ID is recorded as rapid-onset-dystonia-parkinsonism[22].
- dystonia 12's UniProt disease ID is recorded as DI-00419[23].