dentatorubral-pallidoluysian atrophy
congenital disorder of nervous system
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Summary
dentatorubral-pallidoluysian atrophy is a rare disease[1]. It draws 473 Wikipedia views per month (rare disease category, ranking #202 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: spinocerebellar ataxia[4], autosomal dominant cerebellar ataxia type IV[5], Huntington's disease-like syndrome[6]
- Prevalence: 0.000005[7]
- ICD-9-CM: 333.99[8]
- NCI Thesaurus ID: C7636[9], C122653[10]
- Health specialty: neurology[11]
- Genetic association: ATN1[12]
- Age of onset: any age[13]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060162[14], http://identifiers.org/doid/DOID:0060162[15], http://www.orpha.net/ORDO/Orphanet_101[16]
- On focus list of Wikimedia project: WikiProject Medicine[17]
- Has phenotype: Q141815138[18], ophthalmoplegia[19], pathologic nystagmus[20], hereditary optic neuropathy[21], dysarthria[22], hyporeflexia[23], Choreoathetosis[24], dysmetria[25], ataxia[26], Dysdiadochokinesia[27], truncal ataxia[28], Action tremor[29], involuntary movement[30], impaired proprioception[31]
- P14914: D00101[32]
Why It Matters
dentatorubral-pallidoluysian atrophy has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[33] It is known by 23 alternative names across languages and contexts.[34]