Gaucher s disease, for example, is a rare crippling genetic condition that, in its more severe forms, usually killed its victims in childhood.

Rare Serum sickness Very rare Anaphylaxis

the common disease or the rare disease?

This isn't a genetic disease.

Cystic fibrosis is a genetic disease.

Liver disease (hepatitis) (rare)

It's seen as a genetic disease.

Other side effects Some patients have had the following side effects while taking Jalra and metformin Common

Worsening of a condition called myasthenia gravis, a rare disease which causes muscle

personal or family history of hereditary muscular disorders

if you have porphyria (an uncommon metabolic disorder)

Whipple's disease is a rare, systemic infectious disease caused by the bacterium Tropheryma whipplei .

Gaucher disease is a rare inherited disorder.

Soliris is used to treat patients with paroxysmal nocturnal haemoglobinuria (PNH), a rare, life threatening genetic disease that causes the red blood cells to be broken down too quickly.

Take special care with Zyrtec If you are a patient with renal insufficiency.

if you have rare hereditary problems of fructose intolerance

So let's think about a disease that affects it's pretty rare, it affects one person in 10,000.

Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome.

Replagal is used to treat patients who have Fabry disease, a rare inherited disorder.

In fact, if we look at the genetic code, it's the only disease we can see that people who lived in Africa

Fabrazyme is used to treat patients who have Fabry disease, a rare inherited disorder.

We can prove that we understand the genetic structure of a human disease by synthesizing the same disease in a mouse.

Xanthinuria is a rare genetic disorder where the lack of xanthine oxidase leads to high concentration of xanthine in blood and can cause health problems such as renal failure.

Myozyme is used to treat patients who have Pompe disease, a rare inherited disorder.

Common, the common I think that's absolutely right, and why?

Cardiovascular disease Type 2 diabetes is associated with an increased risk for cardiovascular disease.

CYSTAGON is prescribed to manage this rare inherited disorder.

Immune system disorders Very rare ( 1 10,000) Serum sickness, anaphylaxis, polyarteritis nodosa

So, the website of the National Cancer Institute says that cancer is a genetic disease.

Hyperkalemic periodic paralysis (HYPP, HyperKPP) is a genetic disorder that occurs in horses and humans, where it is also known as Impressive syndrome.

If a hereditary muscular disease is suspected in such patient, restarting statin therapy is not recommended.

Familial Adenomatous Polyposis (FAP) is a genetic disease resulting from an autosomal dominant genetic alteration of a tumor suppressor gene, the adenomatous polyposis coli (APC) gene.

This is a serious disease and there are very few treatments.

if you suffer from myasthenia gravis, a rare disease which causes muscle weakness.

Because the number of people with essential thrombocythaemia is low, the disease is rare, and Xagrid was designated as an orphan medicine (a medicine used in rare disease) on 29 December 2000.

Because the number of patients with hairy cell leukaemia is low, the disease is considered rare , and LITAK was designated an orphan medicine (a medicine used in rare diseases) on 18 September 2001.

In fact, if we look at the genetic code, it's the only disease we can see that people who lived in Africa actually evolved several things to avoid malarial deaths.

Patients with rare hereditary problems of fructose intolerance should not take this medicine.

Such an attitude should not be encouraged by the medical profession for ethical reasons, nor will it ever be able scientifically to satisfy the demands thus created.7 Moreover, this mentality would not only considerably impair our willingness to deal with the disabled but could also produce a shift from allowing prenatal selection to demanding neonatal selection.

Rare Rare Rare Rare Rare Rare Rare

It may be a severe strain for an individual to know that he suffers from an untreatable hereditary illness and it may limit the options open to him.

In late 1995, two young people were diagnosed with Creutzfeldt Jakob disease a rare disease typically seen in elderly patients.

Patients with rare hereditary problems of fructose intolerance should not take this medicine.

Enbrel is not effective in the treatment of Wegener s granulomatosis, a rare inflammatory disease.

Because the disease is rare, many of the children were included in more than one of the studies.