ADan amyloidosis
cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has material basis in an autosomal dominant mutation of ITM2B on chromosome 13q14.2
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ADan amyloidosis
Summary
ADan amyloidosis is a rare disease[1]. It draws 216 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]
Key Facts
- ADan amyloidosis's instance of is recorded as rare disease[3].
- ADan amyloidosis's instance of is recorded as class of disease[4].
- ADan amyloidosis is a type of cerebral amyloid angiopathy[5].
- ADan amyloidosis is a type of ITM2B amyloidosis[6].
- ADan amyloidosis is a type of genetic disease[7].
- ADan amyloidosis's genetic association is recorded as ITM2B[8].
- ADan amyloidosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070030[9].
- ADan amyloidosis's exact match is recorded as http://identifiers.org/doid/DOID:0070030[10].
- ADan amyloidosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97346[11].
- ADan amyloidosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
ADan amyloidosis draws 216 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2] It is known by 12 alternative names across languages and contexts.[13]