Acanthosis Nigricans

Alias:
Keratosis Nigricans
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Acanthosis Nigricans, also known as keratosis nigricans, is related to pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities and familial partial lipodystrophy, and has symptoms including pruritus An important gene associated with Acanthosis Nigricans is PRMT7 (Protein Arginine Methyltransferase 7), and among its related pathways/superpathways are Signal Transduction and TGF-Beta Pathway. The drugs Metformin and Leuprolide have been mentioned in the context of this disorder. Affiliated tissues include skin and ovary, and related phenotypes are acanthosis nigricans and Increased shRNA abundance (Z-score > 2)
Related ID:
MESH:D000052
ICD11:71488193

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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21
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Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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