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Diseases » T-cell lymphoma 1A » Summary

What is T-cell lymphoma 1A?

What is T-cell lymphoma 1A?

  • T-cell lymphoma 1A: T-cell lymphoma 1A is a type of cancer that has genetic origins. The genetic defect is located on chromosome 14q32.1. The anomaly is usually implicated in t-cell prolymphocytic leukemia. The cancer is usually aggressive and tends to target the blood, bone marrow, lymph nodes, liver, spleen and skin. The cancer is generally quite rare and tends to occur in people over the age of 30.

T-cell lymphoma 1A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that T-cell lymphoma 1A, or a subtype of T-cell lymphoma 1A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

T-cell lymphoma 1A: Introduction

Types of T-cell lymphoma 1A:

Broader types of T-cell lymphoma 1A:

What causes T-cell lymphoma 1A?

Causes of T-cell lymphoma 1A: see causes of T-cell lymphoma 1A

What are the symptoms of T-cell lymphoma 1A?

Symptoms of T-cell lymphoma 1A: see symptoms of T-cell lymphoma 1A

T-cell lymphoma 1A: Testing

Diagnostic testing: see tests for T-cell lymphoma 1A.

Misdiagnosis: see misdiagnosis and T-cell lymphoma 1A.

How is it treated?

Treatments for T-cell lymphoma 1A: see treatments for T-cell lymphoma 1A

Name and Aliases of T-cell lymphoma 1A

Main name of condition: T-cell lymphoma 1A

Other names or spellings for T-cell lymphoma 1A:


Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)


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