All diseases

OMIM ID
278000
OMIM term:
LYSOSOMAL ACID LIPASE DEFICIENCY
Alternative terms:
CHOLESTERYL ESTER STORAGE DISEASE; CESD
LIPA DEFICIENCY
LAL DEFICIENCY CHOLESTEROL ESTER HYDROLASE DEFICIENCY WOLMAN DISEASE, INCLUDED
(∗) Location:
10q23.31  
(†) Associated OMIM genes:
LIPA  
(‡) Associated MGI genes:
Lipa  

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