Wolman disease
(Q6710283)
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme
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Current Data About
Wolman disease
| (P31) |
(Q112193867)
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| (P138) |
(Q6916185)
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| (P279) |
(Q53660462)
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| (P373) |
Lysosomal acid lipase deficiency
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| (P1748) |
C61271
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| (P1995) |
(Q162606)
(Q668064) |
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| (P2293) |
(Q18028580)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_14497
http://identifiers.org/doid/DOID:14497
http://www.orpha.net/ORDO/Orphanet_75233 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Acid esterase deficiency Acid lipase deficiency, NOS Wolman xanthomatosis Wolman's disease (disorder) Wolman's or triglyceride storage type III disease Xanthomatosis, familial Xanthomatosis, familial (disorder) Wolman's disease Acid lipase deficiency LAL-D LAL deficiency |
| description | autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme |
External Links