adult-onset basal ganglia disease
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adult-onset basal ganglia disease
Summary
adult-onset basal ganglia disease is a designated intractable/rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- adult-onset basal ganglia disease's instance of is recorded as designated intractable/rare disease[3].
- adult-onset basal ganglia disease's instance of is recorded as rare disease[4].
- adult-onset basal ganglia disease's instance of is recorded as class of disease[5].
- adult-onset basal ganglia disease is a type of neurodegeneration with brain iron accumulation[6].
- adult-onset basal ganglia disease is a type of Huntington's disease-like syndrome[7].
- adult-onset basal ganglia disease is a type of nervous system heredodegenerative disease[8].
- adult-onset basal ganglia disease is a type of genetic disease[9].
- adult-onset basal ganglia disease is a type of autosomal dominant disease[10].
- adult-onset basal ganglia disease's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4807[11].
- adult-onset basal ganglia disease's ICD-9-CM is recorded as 333.0[12].
- adult-onset basal ganglia disease's health specialty is recorded as neurology[13].
- adult-onset basal ganglia disease's genetic association is recorded as FTL[14].
- adult-onset basal ganglia disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110737[15].
- adult-onset basal ganglia disease's exact match is recorded as http://identifiers.org/doid/DOID:0110737[16].
- adult-onset basal ganglia disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_157846[17].
- adult-onset basal ganglia disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
adult-onset basal ganglia disease has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[19]