Wolman disease

noun

A rare genetic disorder caused by deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA), necessary to break down certain lipids.

Meanings

nounWolman disease (uncountable)
  1. uncountableA rare genetic disorder caused by deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA), necessary to break down certain lipids.

Origin

Named after Moshe Wolman, one of the authors of the first case study, published in 1956.

Full word history & related roots →
Cite this entry
APA

Wolman disease. (n.d.). In WatkinsX Dictionary. Retrieved November 5, 2026, from https://dictionary.watkinsx.com/word/Wolman%20disease

MLA

“Wolman disease.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/Wolman%20disease. Accessed November 5, 2026.

Chicago

WatkinsX Dictionary, s.v. “Wolman disease,” accessed November 5, 2026, https://dictionary.watkinsx.com/word/Wolman%20disease.

Source: Wolman disease on Wiktionary, CC BY-SA 4.0.