dentatorubral-pallidoluysian atrophy
congenital disorder of nervous system
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dentatorubral-pallidoluysian atrophy
Summary
dentatorubral-pallidoluysian atrophy is a rare disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- dentatorubral-pallidoluysian atrophy's instance of is recorded as rare disease[3].
- dentatorubral-pallidoluysian atrophy's instance of is recorded as class of disease[4].
- dentatorubral-pallidoluysian atrophy is a type of spinocerebellar ataxia[5].
- dentatorubral-pallidoluysian atrophy is a type of autosomal dominant cerebellar ataxia type IV[6].
- dentatorubral-pallidoluysian atrophy is a type of Huntington's disease-like syndrome[7].
- dentatorubral-pallidoluysian atrophy's ICD-9-CM is recorded as 333.99[8].
- dentatorubral-pallidoluysian atrophy's NCI Thesaurus ID is recorded as C7636[9].
- dentatorubral-pallidoluysian atrophy's NCI Thesaurus ID is recorded as C122653[10].
- dentatorubral-pallidoluysian atrophy's health specialty is recorded as neurology[11].
- dentatorubral-pallidoluysian atrophy's genetic association is recorded as ATN1[12].
- dentatorubral-pallidoluysian atrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060162[13].
- dentatorubral-pallidoluysian atrophy's exact match is recorded as http://identifiers.org/doid/DOID:0060162[14].
- dentatorubral-pallidoluysian atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101[15].
- dentatorubral-pallidoluysian atrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
dentatorubral-pallidoluysian atrophy has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 16 alternative names across languages and contexts.[17]