hyper-IgD syndrome

Summary

hyper-IgD syndrome is a hereditary disorder^[1]. It draws 2 Wikipedia views per month (hereditary_disorder category, ranking #15 of 25).^[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's subclass of is recorded as hyperimmunoglobulin syndrome^[7].
• hyper-IgD syndrome's OMIM ID is recorded as 260920^[8].
• hyper-IgD syndrome's DiseasesDB is recorded as 30161^[9].
• hyper-IgD syndrome's has cause is recorded as mevalonic aciduria^[10].
• hyper-IgD syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4750^[11].
• hyper-IgD syndrome's Orphanet ID is recorded as 343^[12].
• hyper-IgD syndrome's genetic association is recorded as MVK^[13].
• hyper-IgD syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_343^[14].
• hyper-IgD syndrome's UMLS CUI is recorded as C0398691^[15].
• hyper-IgD syndrome's ICD-10-CM is recorded as E85.0^[16].
• hyper-IgD syndrome's PatientsLikeMe condition ID is recorded as hyper-igd-syndrome^[17].
• hyper-IgD syndrome's GARD rare disease ID is recorded as 2788^[18].
• hyper-IgD syndrome's Mondo ID is recorded as MONDO_0009849^[19].
• hyper-IgD syndrome's UniProt disease ID is recorded as DI-01768^[20].

Why It Matters

hyper-IgD syndrome draws 2 Wikipedia views per month (hereditary_disorder category, ranking #15 of 25).^[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.^[21] It is known by 14 alternative names across languages and contexts.^[22]