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pancreatic triacylglycerol lipase deficiency

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description 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.
Uniprot Description An autosomal recessive disorder characterized by exocrine pancreatic failure. Clinical findings include oily/greasy stools from infancy or early childhood, absence of discernible pancreatic disease, and significantly decreased pancreatic lipolytic activity.
Mondo Term and Equivalent IDs
MONDO:0013700:  pancreatic triacylglycerol lipase deficiency
NCIT:C129030: 
Orphanet:309031: 
SCTID:78960005: 
UMLS:C0268240: