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MIM:245900 - LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
Xenbase Genes: lcat
Human Disease Resource: MIM
MONDO:0009515 - Norum disease |
MONDO:0018999 - LCAT deficiency |
DOID:1391 - Norum disease |
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MONDO:0009515 - Norum disease |
MONDO:0018999 - LCAT deficiency |
DOID:1391 - Norum disease |