Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

5 matching diseasesClear search ×

Pancreatic triacylglycerol lipase deficiency

Pancreatic triglyceride lipase deficiency

ORPHA:309031

Combined pancreatic lipase-colipase deficiency

ORPHA:309111

Hyperlipidemia due to hepatic triacylglycerol lipase deficiency

Hyperlipidemia due to hepatic lipase deficiency · Hyperlipidemia due to HL deficiency

ORPHA:140905

Neutral lipid storage disease with myopathy

Neutral lipid storage disease type M · NLSDM

ORPHA:98908

Pancreatic colipase deficiency

ORPHA:309108