A brief overview of only a few joooooish genetic diseases: Bloom's Syndrome
The characteristics of Bloom's syndrome include shortness in stature, sun-sensitive facial skin lesions, an increased susceptibility to infections, and a higher incidence of leukemia and certain cancers. Intelligence is usually normal. (More)
Canavan Disease
Canavan disease is a progressive neurological disorder whose symptoms begin in infancy with loss of previously attained skills. Findings include abnormal muscle tone (floppiness or stiffness), feeding difficulties, a large, poorly controlled head, and seizures. Those affected frequently die in childhood, but some survive into their teens or early 20s. (More)
Cystic Fibrosis (CF)
Cystic fibrosis is a chronic, progressive disorder causing the body to produce thick, sticky mucus that clogs the lungs and impairs other organ functions. While severity is variable, most affected individuals face frequent lung infections, fat malabsorption, poor growth, and infertility in males. The median age of survival is in the mid-30s. CF does not affect intelligence. (More)
Familial Dysautonomia (FD)
In individuals with FD, the autonomic and sensory nervous systems malfunction. Symptoms vary, and may include insensitivity to pain, unstable blood pressure and body temperature, absence of overflow tears, frequent pneumonia, and poor growth. FD is often associated with a shortened lifespan. (More)
Fanconi Anemia Type C
Symptoms of this chronic blood disorder include bone marrow failure, short stature, and a predisposition to cancers such as leukemia. Some children affected by Fanconi anemia Type C may have heart, kidney, and limb abnormalities, and learning difficulties or mental retardation. (More)
Gaucher Disease Type 1
In Gaucher disease Type 1, the age of onset and the progression of the symptoms vary. The most common features include an enlarged liver and spleen, anemia, easy bruising, bone pain, and fatigue. Treatment for Gaucher disease is available. (More)
Glycogen Storage Disorder Type 1a (GSD1a)
GSD1a is a metabolic disorder that causes poor blood sugar maintenance, growth failure, anemia, an enlarged liver, and may interfere with kidney and pancreatic function. Disease management involves lifelong diet modification. (More)
Maple Syrup Urine Disease (MSUD)
Named for the characteristic maple syrup smell of the urine in affected individuals, MSUD is a disorder of amino acid metabolism. The condition is variable and affects newborns with irritability, poor feeding, lethargy, seizures, and coma, in addition to the urine odor. With careful dietary control, normal growth and development are possible. (More)
Mucolipidosis IV (ML4)
ML4 is a neurological disorder with symptoms beginning in infancy, often confused with cerebral palsy. Characteristics include spasticity, mental retardation and severe visual problems. The severity of the disorder and the lifespan vary. Patients have elevated serum gastrin levels. (More)
Niemann-Pick Disease Type A
Niemann-Pick disease Type A is a neurodegenerative disorder whose symptoms include enlargement of the liver and spleen, poor growth, and progressive mental and physical deterioration. Life expectancy is about two to four years of age. (More)
Tay-Sachs Disease
Tay-Sachs disease is a progressive, neurological condition that begins during infancy. Deterioration of the central nervous system becomes apparent at about six months of age. Symptoms include loss of coordination, blindness, deafness, seizures, and severe mental retardation. The average life expectancy is about three to five years. Rarer than the infantile type is Late Onset Tay-Sachs disease, where the progression of symptoms is slower and milder. (More on Tay-Sachs Infantile) (More on Tay-Sachs Late Onset)
And what are the diseases peculiar to Northern Europeans? HHC IS AN INHERITED GENETIC DISEASE
“Hereditary Hemochromatosis is a genetic disease that is the result of inheriting two defective copies of a particular gene, one from each parent. The mutation in this gene causes the intestine to absorb too much iron. Over time, usually several years, this excess iron is deposited in the cells of the liver, heart, pancreas, joints, and pituitary gland. If left untreated, organ damage can result.” – Center for Disease Control, Atlanta, USA
http://www.cdc.gov/nccdphp/dnpa/Hemochromatosis/faq.htm“Hemochromatosis is a genetic disease, often most prevalent among people of northern European descent. This means that Hemochromatosis is inherited. A person will be born with Hemochromatosis only if two Hemochromatosis genes are inherited - one from the mother and one from the father.” – University of Maryland, USA,
http://www.umm.edu/blood/hemachro.htm HHC IS FOUND ONLY AMONGST EUROPEANS
The Center for Disease Control confirms that HHC is an exclusively European disease:
“In the general population, the frequency of the C282Y/C282Y genotype is 0.4%. C282Y heterozygosity ranges from 9.2% in Europeans to nil in the Asian, Indian subcontinent, African/Middle Eastern, and Australasian populations.” – CDC, “HFE Gene and Hereditary Hemochromatosis” by E. H. Hanson, G. Imperatore, W. Burke, March 12, 2001 (Updated)
http://www.cdc.gov/genetics/hugenet/reviews/HFE.htmAnd the funny thing is, when I looked at other diseases that affect so-called Whites, they were jooooish diseases; not diseases that affect Israelites.
So exactly who is superior here? The jooos would have us and the rest of the biped population, riddled with diseases like them. Misery loves company.
Ye chosen seed of Israel's race, ye ransomed from the fall, hail him who saves you by his grace, and crown him Lord of all. Hail him who saves you by his grace, and crown him Lord of all.