Essential Thrombocythemia (ET)

Alias:
Essential Thrombocytosis
Hemorrhagic Thrombocythemia
Hereditary Thrombocythemia
Thrombocythemia, Essential
Familial Thrombocytosis
Primary Thrombocytosis
Et
Essential Thrombocythaemia
Thrombocythemia Essential
Familial Thrombocythemia
Primary Thrombocythemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Essential Thrombocythemia, also known as essential thrombocytosis, is related to thrombocythemia 1 and acquired von willebrand syndrome. An important gene associated with Essential Thrombocythemia is MPL (MPL Proto-Oncogene, Thrombopoietin Receptor), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Benzocaine and Tannic acid have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and myeloid, and related phenotypes are myocardial infarction and venous thrombosis
Related ID:
MESH:D013920

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
XL
All ages
1-5/10000
72
987
36

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
No Data Found!
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