Wolman disease (Q6710283)
(Redirected from Q2061846)
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
- Acid esterase deficiency
- Acid lipase deficiency, NOS
- Wolman xanthomatosis
- Wolman's disease (disorder)
- Wolman's or triglyceride storage type III disease
- Xanthomatosis, familial
- Xanthomatosis, familial (disorder)
- Wolman's disease
- Acid lipase deficiency
- LAL-D
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Wolman disease |
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme |
|
Statements
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C61271
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Lysosomal acid lipase deficiency
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Identifiers
Wolman Disease
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Sitelinks
Wikipedia(12 entries)
- arwiki داء ولمان
- bswiki Wolmanov sindrom
- dewiki Wolman-Krankheit
- enwiki Lysosomal acid lipase deficiency
- eswiki Enfermedad de Wolman
- fawiki بیماری ولمن
- fiwiki Wolmanin tauti
- frwiki Maladie de Wolman
- itwiki Malattia di Wolman
- plwiki Choroba Wolmana
- ruwiki Болезнь Вольмана
- svwiki Kolesterolesterlagringsdefekt
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
Wikisource(0 entries)
Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Lysosomal acid lipase deficiency