Terminology Service for NFDI4Health
Combined Lipase Deficiency
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http://purl.obolibrary.org/obo/NCIT_C126558
A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders. [ ]
Term info
Label
Combined Lipase Deficiency
Synonyms
- Combined Lipase Deficiency
Preferred Name
Combined Lipase Deficiency
Semantic Type
Disease or Syndrome
UMLS CUI
C1855498
code
C126558