transthyretin amyloidosis
HEREDITARY AMYLOIDOSIS
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transthyretin amyloidosis
Summary
transthyretin amyloidosis is a rare disease[1]. It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- transthyretin amyloidosis's instance of is recorded as rare disease[3].
- transthyretin amyloidosis's instance of is recorded as class of disease[4].
- transthyretin amyloidosis is a type of amyloidosis[5].
- transthyretin amyloidosis is a type of familial amyloid neuropathy[6].
- transthyretin amyloidosis is a type of autosomal dominant disease[7].
- transthyretin amyloidosis is a type of hereditary ATTR amyloidosis[8].
- transthyretin amyloidosis is a type of disease[9].
- transthyretin amyloidosis's Commons category is recorded as Familial amyloid polyneuropathy[10].
- transthyretin amyloidosis's ICD-9-CM is recorded as 277.39[11].
- transthyretin amyloidosis's NCI Thesaurus ID is recorded as C84555[12].
- transthyretin amyloidosis's NCI Thesaurus ID is recorded as C84554[13].
- transthyretin amyloidosis's health specialty is recorded as neurology[14].
- transthyretin amyloidosis's genetic association is recorded as TTR[15].
- transthyretin amyloidosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050638[16].
- transthyretin amyloidosis's exact match is recorded as http://identifiers.org/doid/DOID:0050638[17].
- transthyretin amyloidosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
transthyretin amyloidosis has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2] It is known by 33 alternative names across languages and contexts.[19]