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Disease association ontology term - MONDO:0019148 - Wolman disease

Term summary

ID
MONDO:0019148
Name
Wolman disease
Ontology or CV name
Disease association
Definition
Wolman disease represents the most severe manifestation of lysosomal acid lipase deficiency. Milder phenotypes as a whole are referred to as cholesterol ester storage disease. The acid lipase enzyme plays an essential role in lysosomal hydrolysis of both esterified cholesterol and triglycerides of lipoproteic origin. In Wolman disease, the rarest form of acid lipase deficiency, these lipids accumulate in most tissues.

Parents

Annotation

Disease association

MONDO:0019148 - Wolman disease

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