Lipase deficiency, combined
MONDO:0009527A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders.
Also known as: combined lipase deficiency, familial lipase maturation factor 1 deficiency, lipase deficiency, combined, LPL and HL deficiency, LPL and HTGL deficiency, lipase deficiency combined, lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency
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Disease
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Hereditary disease
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Syndromic disease
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Human disease
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Familial chylomicronemia syndrome
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Autosomal recessive disease
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Disease of genetic or genomic mechanism
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Autosomal genetic disease
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