| Disease Aliases (33) | Acid cholesteryl ester hydrolase deficiency, wolman type Acid lipase deficiency Acid cholesteryl ester hydrolase deficiency, type 2 Acid esterase deficiency Acid lipase disease Cesd Cholesterol ester hydrolase deficiency Cholesteryl ester storage disease Disease, wolman Disease, wolman's Familial xanthomatoses Familial xanthomatosis Lal (lysosomal acid lipase) deficiency Lal deficiency Lald - lysosomal acid lipase deficiency Lipa deficiency Liposomal acid lipase deficiency, wolman type Wolman xanthomatosis Wolman's disease Wolman's xanthomatosis Wolman's or triglyceride storage type iii disease Wolmans disease Xanthomatoses, familial Xanthomatosis, familial Xanthomatosis, wolman Xanthomatosis, wolman's Xanthomatosis, wolmans Deficiency of cholesterol esterase and triacylglycerol lipase Familial visceral xanthomatosis Lysosomal acid lipase deficiency Primary familial xanthomatosis Primary familial xanthomatosis with adrenal calcification |
Associated Genes (1) NCBI-RefSeq: LIPA (Lipase A, lysosomal acid type) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Wolman disease | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |