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Familial Wilms tumor 2

Familial Wilms tumor 2: Introduction

Familial Wilms tumor 2: A familial form malignant kidney tumor that occurs in children. Type 2 differs from other forms of Wilms tumor by the origin of the genetic defect (chromosome 19q13.4). More detailed information about the symptoms, causes, and treatments of Familial Wilms tumor 2 is available below.

Symptoms of Familial Wilms tumor 2

Treatments for Familial Wilms tumor 2

Home Diagnostic Testing

Home medical testing related to Familial Wilms tumor 2:

Wrongly Diagnosed with Familial Wilms tumor 2?

Familial Wilms tumor 2: Complications

Review possible medical complications related to Familial Wilms tumor 2:

Causes of Familial Wilms tumor 2

Read more about causes of Familial Wilms tumor 2.

Familial Wilms tumor 2: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Familial Wilms tumor 2

Chronic digestive conditions often misdiagnosed: When diagnosing chronic symptoms of the digestive tract, there are a variety of conditions that may be misdiagnosed. The best known, irritable bowel syndrome, is over-diagnosed, more »

Intestinal bacteria disorder may be hidden cause: One of the lesser known causes of diarrhea is an imbalance of bacterial in the gut, sometimes called more »

Antibiotics often causes diarrhea: The use of antibiotics are very likely to cause some level of diarrhea in patients. The reason is that antibiotics kill off not only "bad" bacteria, but can also kill the more »

Food poisoning may actually be an infectious disease: Many people who come down with "stomach symptoms" like diarrhea assume that it's "something I ate" (i.e. food poisoning) more »

Mesenteric adenitis misdiagnosed as appendicitis in children: Because appendicitis is one of the more feared conditions for a child with abdominal pain, it can be over-diagnosed (it can, of course, also fail to be diagnosed with fatal more »

Spitz nevi misdiagnosed as dangerous melanoma skin cancer: One possible misdiagnosis to consider in lieu of melanoma is spitz nevi. See melanoma and spitz more »

Interstitial cystitis an under-diagnosed bladder condition: The medical condition of interstitial cystitic is a bladder condition that can be misdiagnosed as more »

Celiac disease often fails to be diagnosed cause of chronic digestive symptoms: One of the most common chronic digestive conditions is celiac disease, a malabsorption disorder with a variety of symptoms (see symptoms of celiac disease) more »

Chronic digestive diseases hard to diagnose: There is an inherent difficulty in diagnosing the various types of chronic digestive diseases. Some of the better known possibilities are peptic ulcer, colon cancer, more »

Familial Wilms tumor 2: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Familial Wilms tumor 2

Research quality ratings and patient safety measures for medical facilities in specialties related to Familial Wilms tumor 2:

Choosing the Best Hospital: More general information, not necessarily in relation to Familial Wilms tumor 2, on hospital performance and surgical care quality:

Familial Wilms tumor 2: Rare Types

Rare types of diseases and disorders in related medical categories:

Familial Wilms tumor 2: Animations

Prognosis for Familial Wilms tumor 2

Prognosis for Familial Wilms tumor 2: Early detection improves prognosis.

Statistics for Familial Wilms tumor 2

Familial Wilms tumor 2: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Familial Wilms tumor 2, or answer someone else's question, on our message boards:

Definitions of Familial Wilms tumor 2:

Familial Wilms tumor 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Familial Wilms tumor 2, or a subtype of Familial Wilms tumor 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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