Farber lipogranulomatosis
extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase
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Summary
Farber lipogranulomatosis is a rare disease[1]. It ranks in the top 0.64% of rare_disease entities by monthly Wikipedia readership (98 views/month, #4 of 627).[2]
Key Facts
- Farber lipogranulomatosis is credited with the discovery of Sidney Farber[3].
- Farber lipogranulomatosis's instance of is recorded as rare disease[4].
- Farber lipogranulomatosis's instance of is recorded as class of disease[5].
- Farber lipogranulomatosis is a type of lipid storage disease[6].
- Farber lipogranulomatosis is a type of genetic disease[7].
- Farber lipogranulomatosis's described by source is recorded as The Unified Medical Dictionary (Librairie du Liban, 2009)[8].
- Farber lipogranulomatosis's NCI Thesaurus ID is recorded as C84710[9].
- Farber lipogranulomatosis's health specialty is recorded as endocrinology[10].
- Farber lipogranulomatosis's genetic association is recorded as ASAH1[11].
- Farber lipogranulomatosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050464[12].
- Farber lipogranulomatosis's exact match is recorded as http://identifiers.org/doid/DOID:0050464[13].
- Farber lipogranulomatosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Body
Works and Contributions
Farber lipogranulomatosis is credited with the discovery of Sidney Farber[3].
Why It Matters
Farber lipogranulomatosis ranks in the top 0.64% of rare_disease entities by monthly Wikipedia readership (98 views/month, #4 of 627).[2] It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[15] It is known by 32 alternative names across languages and contexts.[16]