Juvenile Xanthogranuloma

Alias:
Multiple Eruptive Juvenile Xanthogranuloma
Xanthogranuloma, Juvenile
Naevoxanthoendothelioma
Xanthoma Neviforme
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Juvenile Xanthogranuloma, also known as multiple eruptive juvenile xanthogranuloma, is related to histiocytosis and cutaneous fibrous histiocytoma, and has symptoms including exanthema and pruritus. An important gene associated with Juvenile Xanthogranuloma is FSCN1 (Fascin Actin-Bundling Protein 1), and among its related pathways/superpathways are Innate Immune System and Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell. The drugs Vemurafenib and Palbociclib have been mentioned in the context of this disorder. Affiliated tissues include skin and lung, and related phenotypes are glaucoma and multiple cafe-au-lait spots
Related ID:
MESH:D014972
ICD11:98595592

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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14
238
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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