Cowden Syndrome (CD)

Alias:
Cowden Disease
Multiple Hamartoma Syndrome
Lhermitte-Duclos Disease
Cowden's Disease
Dysplastic Gangliocytoma of Cerebellum
Hamartoma Syndrome, Multiple
Cowden's Syndrome
Mham
Cs
Cd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cowden Syndrome, also known as cowden disease, is related to cowden syndrome 1 and cowden syndrome 4, and has symptoms including seizures, action tremor and cerebellar ataxia. An important gene associated with Cowden Syndrome is PTEN (Phosphatase And Tensin Homolog), and among its related pathways/superpathways are Signal Transduction and Prolactin Signaling. The drugs Everolimus and Temsirolimus have been mentioned in the context of this disorder. Affiliated tissues include thyroid and breast, and related phenotypes are generalized hyperkeratosis and palmoplantar keratoderma
Related ID:
MESH:D006223

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
1-9/1000000
89
1322
54

Medical Symptom

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

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
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