Jewish racial disease Variations
Overrepresentation of rare variants in a specific racial group, i.e., JEWS, should not confuse interpretation of medical association analyses. Only the Jews, as a race, carry these genetic disorders. The Jews are a race and not a religion!
Scientific investigators have found that these diseases are more severe among Jews originating from North Africa than among Jews from Iran, Iraq or Turkey. The incidence of diseases particular to the Jewish race is believed to mirror regional variations, with the fewest cases reported among Ashkenazi Jews or Jews from Eastern and Western Europe.
North African Jews also tended to have more severe manifestations of other symptoms diseases, including arthritis, vasculitis and deep vein thrombosis and negroid-lip appearance.
As an example, the disease Tay-Sachs is a racial mutation named after British ophthalmologist Warren Tay, who in 1881 first described a symptomatic red spot on the retina of the eye; and American neurologist Bernard Sachs, who found the disease in Ashkenazi Jews has mutated to all Jews. Here’s the list of racial Jewish diseases. Do Catholics, Lutherans, Baptist, etc. have common diseases? NO! The Jews are a race and not a religion!
A list of sick degenerate Jewish racial diseases:
Diseases Common to all Jewish Groups
Glycogen Storage Disease Type II
Phenylalanine Hydroxylase Deficiency
Ashkenazi Jewish Diseases
3-Phosphoglycerate Dehydrogenase Deficiency
Arthrogryposis, Mental Retardation and Seizures
Carnitine Palmitoyltransferase ll Deficiency
Congenital Amegakaryocytic Thrombocytopenia
Congenital Disorder of Glycosylation la
Deafness-Autosomal Recessive 77
Dyskeratosis Congenita, Autosomal Recessive
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IV / Adult Polyglucosan Body Disease
Glycogen Storage Disease Type VII
Lipoamide Dehydrogenase Deficiency
Mitochondrial Complex 1 Deficiency
Multiple Sulphatase Deficiency
Phenylalanine Hydroxylase Deficiency
Polycystic Kidney Disease, Autosomal Recessive
Pontocerebellar Hypoplasia Type 1A
Primary Ciliary Dyskinesia DNAH5
Primary Ciliary Dyskinesia DNAI1
Primary Ciliary Dyskinesia DNAI2
Walker Warburg Syndrome and Other FKTN-Related Dystrophies
Zellweger Syndrome Spectrum-PEX2
Sephardi-Mizrahi Jewish Diseases
3-Methylglutaconic Aciduria, Type III / Optic Atrophy 3, with Cataract
Adrenoleukodystrophy-X-Linked ABCD1
Asparagine Synthetase Deficiency
Beta-Globin-Related Hemoglobinopathies
Cerebrotendinous Xanthomatosis
Congenital Insensitivity to Pain with Anhidrosis
Congenital Myasthenic Syndrome
Corticosterone Methyloxidase Deficiency
Glycogen Storage Disease Type II
Glycogen Storage Disease Type III
Glycogen Storage Disease Type V
GNE Myopathy (Hereditary Inclusion Body Myopathy)
Hereditary Spastic Paraparesis 49
Homocystinuria due to MTHFR Deficiency
Infantile Cerebral and Cerebellar Atrophy
Leber Congenital Amaurosis 2-Retinitis Pigmentosa 20
Limb Girdle Muscular Dystrophy Type 2B
Megalencephalic Leukoencephalopathy with Subcortical Cysts
Mitochondrial Complex 1 Deficiency
Mitochondrial Myopathy and Sideroblastic Anemia
Myoneurogastrointestinal Encephalopathy
Ornithine Aminotransferase Deficiency
Phenylalanine Hydroxylase Deficiency
Polyglandular Autoimmune Syndrome, Type I
Pontocerebellar Hypoplasia Type 6
Progressive Cerebello-Cerebral Atrophy
Renal Tubular Acidosis and Deafness
Wolman Disease / Cholesteryl Ester Storage Disease