Wolman disease
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
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Wolman disease
Summary
Wolman disease is a class of disease[1]. It draws 54 Wikipedia views per month (class_of_disease category, ranking #609 of 1,968).[2]
Key Facts
- Wolman disease's instance of is recorded as class of disease[3].
- Moshe Wolman is named after Wolman disease[4].
- Wolman disease is a type of lysosomal and lipase deficiency[5].
- Wolman disease's Commons category is recorded as Lysosomal acid lipase deficiency[6].
- Wolman disease's NCI Thesaurus ID is recorded as C61271[7].
- Wolman disease's health specialty is recorded as endocrinology[8].
- Wolman disease's health specialty is recorded as hepatology[9].
- Wolman disease's genetic association is recorded as LIPA[10].
- Wolman disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14497[11].
- Wolman disease's exact match is recorded as http://identifiers.org/doid/DOID:14497[12].
- Wolman disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75233[13].
- Wolman disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Wolman disease draws 54 Wikipedia views per month (class_of_disease category, ranking #609 of 1,968).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[15] It is known by 14 alternative names across languages and contexts.[16]