Tangier disease
extremely rare inherited human disorder
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Tangier disease
Summary
Tangier disease is a designated intractable/rare disease[1]. It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Tangier disease's instance of is recorded as designated intractable/rare disease[3].
- Tangier disease's instance of is recorded as rare disease[4].
- Tangier disease's instance of is recorded as class of disease[5].
- Tangier is named after Tangier disease[6].
- Tangier disease is a type of hypolipoproteinemia[7].
- Tangier disease is a type of neurometabolic disease[8].
- Tangier disease is a type of hypoalphalipoproteinemia[9].
- Tangier disease is a type of rare hereditary metabolic disease with peripheral neuropathy[10].
- Tangier disease is a type of rare hereditary systemic disease with peripheral neuropathy[11].
- Tangier disease's Commons category is recorded as Tangier disease[12].
- Tangier disease's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4585[13].
- Tangier disease's NCI Thesaurus ID is recorded as C85182[14].
- Tangier disease's health specialty is recorded as endocrinology[15].
- Tangier disease's genetic association is recorded as ABCA1[16].
- Tangier disease's genetic association is recorded as APOA1[17].
- Tangier disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1388[18].
- Tangier disease's exact match is recorded as http://identifiers.org/doid/DOID:1388[19].
- Tangier disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_31150[20].
- Tangier disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Tangier disease has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2] It is known by 13 alternative names across languages and contexts.[22]