Mannosidosis
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Mannosidosis
Summary
Mannosidosis is a rare disease[1]. Mannosidosis draws 4 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]
Key Facts
- Mannosidosis's instance of is recorded as rare disease[3].
- Mannosidosis's subclass of is recorded as glycoproteinosis[4].
- Mannosidosis's MeSH descriptor ID is recorded as D044904[5].
- Mannosidosis's GeneReviews ID is recorded as NBK1396[6].
- Mannosidosis's MeSH tree code is recorded as C16.320.565.202.607[7].
- Mannosidosis's MeSH tree code is recorded as C16.320.565.595.577[8].
- Mannosidosis's MeSH tree code is recorded as C18.452.648.202.607[9].
- Mannosidosis's MeSH tree code is recorded as C18.452.648.595.577[10].
- Mannosidosis's Orphanet ID is recorded as 61[11].
- Mannosidosis's NCI Thesaurus ID is recorded as C61275[12].
- Mannosidosis's health specialty is recorded as pediatrics[13].
- Mannosidosis's health specialty is recorded as endocrinology[14].
- Mannosidosis's UMLS CUI is recorded as C1257960[15].
- Mannosidosis's GARD rare disease ID is recorded as 6968[16].
- Mannosidosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- Mannosidosis's Microsoft Academic ID is recorded as 2776837302[18].
- Mannosidosis's ICD-11 ID is recorded as 1193907152[19].
Why It Matters
Mannosidosis draws 4 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2] Mannosidosis has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[20] Mannosidosis is known by 4 alternative names across languages and contexts.[21]