Whipple Disease

Alias:
Intestinal Lipodystrophy
Whipple's Disease
Intestinal Lipophagic Granulomatosis
Whipples Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Whipple Disease, also known as intestinal lipodystrophy, is related to aortic valve insufficiency and olecranon bursitis. An important gene associated with Whipple Disease is IRF4 (Interferon Regulatory Factor 4), and among its related pathways/superpathways are Hematopoietic Stem Cells and Lineage-specific Markers and IL27-mediated signaling events. Affiliated tissues include heart and brain, and related phenotypes are depression and developmental regression
Related ID:
MESH:D008061

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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No data available Phase
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17
179
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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