dystonia 16
Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism
Press Enter · cited answer in seconds
0 sources
dystonia 16
Summary
dystonia 16 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- dystonia 16's instance of is recorded as rare disease[3].
- dystonia 16's instance of is recorded as class of disease[4].
- dystonia 16 is a type of multifocal dystonia[5].
- dystonia 16 is a type of rare parkinsonian syndrome due to genetic neurodegenerative disease[6].
- dystonia 16 is a type of persistent combined dystonia[7].
- dystonia 16 is a type of genetic disease[8].
- dystonia 16 is a type of autosomal recessive disease[9].
- dystonia 16's NCI Thesaurus ID is recorded as C168729[10].
- dystonia 16's health specialty is recorded as neurology[11].
- dystonia 16's genetic association is recorded as PRKRA[12].
- dystonia 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090048[13].
- dystonia 16's exact match is recorded as http://identifiers.org/doid/DOID:0090048[14].
- dystonia 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
dystonia 16 is known by 7 alternative names across languages and contexts.[2]