dystonia 9
human disease
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dystonia 9
Summary
dystonia 9 is a rare disease[1].
Key Facts
- dystonia 9's instance of is recorded as rare disease[2].
- dystonia 9's instance of is recorded as class of disease[3].
- dystonia 9's subclass of is recorded as dystonia[4].
- dystonia 9's subclass of is recorded as paroxysmal dystonia[5].
- dystonia 9's subclass of is recorded as genetic disease[6].
- dystonia 9's subclass of is recorded as autosomal dominant disease[7].
- dystonia 9's MeSH descriptor ID is recorded as C563401[8].
- dystonia 9's OMIM ID is recorded as 601042[9].
- dystonia 9's Disease Ontology ID is recorded as DOID:0090044[10].
- dystonia 9's Orphanet ID is recorded as 53583[11].
- dystonia 9's health specialty is recorded as neurology[12].
- dystonia 9's genetic association is recorded as GLUT1[13].
- dystonia 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090044[14].
- dystonia 9's exact match is recorded as http://identifiers.org/doid/DOID:0090044[15].
- dystonia 9's UMLS CUI is recorded as C1832855[16].
- dystonia 9's ICD-10-CM is recorded as G24.8[17].
- dystonia 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- dystonia 9's Mondo ID is recorded as MONDO_0010983[19].
- dystonia 9's UniProt disease ID is recorded as DI-03550[20].