World Of Taxonomy
C129030Level 6

Pancreatic Lipase Deficiency

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive disorder caused by mutation(s) in the PNLIP gene, encoding pancreatic triacylglycerol lipase. The condition is characterized by absent or reduced pancreatic lipase.

**Synonyms:** - PNLIPD

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