Farber lipogranulomatosis
extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase
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Farber lipogranulomatosis
Summary
Farber lipogranulomatosis is a genetic disease[1]. It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Farber lipogranulomatosis is credited with the discovery of Sidney Farber[3].
- Farber lipogranulomatosis's instance of is recorded as genetic disease[4].
- Farber lipogranulomatosis's instance of is recorded as rare disease[5].
- Farber lipogranulomatosis's instance of is recorded as class of disease[6].
- Farber lipogranulomatosis is a type of lipid storage disease[7].
- Farber lipogranulomatosis is a type of disease[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 has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2] It is known by 18 alternative names across languages and contexts.[15]