hyper-IgD syndrome
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hyper-IgD syndrome
Summary
hyper-IgD syndrome is a hereditary disorder[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- hyper-IgD syndrome's instance of is recorded as hereditary disorder[3].
- hyper-IgD syndrome's instance of is recorded as designated intractable/rare disease[4].
- hyper-IgD syndrome's instance of is recorded as rare disease[5].
- hyper-IgD syndrome's instance of is recorded as class of disease[6].
- hyper-IgD syndrome is a type of hyperimmunoglobulin syndrome[7].
- hyper-IgD syndrome's has cause is recorded as mevalonic aciduria[8].
- hyper-IgD syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4750[9].
- hyper-IgD syndrome's genetic association is recorded as MVK[10].
- hyper-IgD syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_343[11].
Why It Matters
hyper-IgD syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[12]