Werner Syndrome (WRN)

Alias:
Adult Progeria
Ws
Werner's Syndrome
Wrn
Adult Premature Ageing Syndrome
Adult Premature Aging Syndrome
Werners Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Werner Syndrome, also known as adult progeria, is related to xeroderma pigmentosum, complementation group g and familial retinoblastoma. An important gene associated with Werner Syndrome is WRN (WRN RecQ Like Helicase), and among its related pathways/superpathways are Gene expression (Transcription) and Infectious disease. The drugs Insulin and Insulin, Globin Zinc have been mentioned in the context of this disorder. Affiliated tissues include skin and thyroid, and related phenotypes are cataract and short stature
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Adolescent
1-9/1000000
37
572
124

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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