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Wolman disease
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
LIPA
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Pathway Enrichment
Most Correlated Biogroups
Lipase, eukaryotic
SILIGAN_TARGETS_OF_EWS_FLI1_FUSION_UP
MODULE_401
LIU_TARGETS_OF_VMYB_VS_CMYB_UP
MODULE_417
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Autosomal recessive hereditary disorder
OMIM - Metabolic diseases
OMIM - Congenital disorder
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Literature
Most Relevant Literature
First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease.
Wolman disease presenting with hemophagocytic lymphohistiocytosis syndrome and a novel LIPA gene var…
Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly.
Enzyme replacement therapy and hematopoietic stem cell transplant: a new paradigm of treatment in Wo…
Sebelipase alfa enzyme replacement therapy in Wolman disease: a nationwide cohort with up to ten yea…
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Clinical Trials
Most Relevant Clinical Trials
Biomarker for Wolman Disease (BioWolman)
A Retrospective Natural History Study of Patients With Lysosomal Acid Lipase Deficiency/Wolman Pheno…
Wolman/CESD Natural History Chart Review and Longitudinal Follow-Up
An Observational Study of Patients With Lysosomal Acid Lipase Deficiency/Cholesteryl Ester Storage D…
Lysosomal Acid Lipase Activity in Nonalcoholic Fatty Liver Disease
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