Wolman disease

短语

释义与例句

n.
  1. 1.

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

    不可数

词源

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

来源：wiktionary