Amalgam and Chronic Diseases, is there a connection?
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Independent Chemist, M.Sc., retired 08.06.2003.
Speciality: Amalgam and Chronic Diseases
Updated version of my peer-reviewed paper, ref. (7), sent to FDA on May 31st, 2003 after the Congressional Hearing on May 8, organized by Congress Members Diane Watson and Dan Burton due to their proposal to ban Amalgam and vaccines containing thiomersal.
THE REAL SCIENTIFIC TRUTH OF AMALGAM, THE BEHAVIOUR OF MERCURY IN THE BODY CAUSING CHRONIC DISEASES.
- INTRODUCTION.
Amalgam is the largest non controlled experiment ever, completely out of step with medical standards. To observe what happens to a cohort of humans, now close to old age, forced to go through life with implants in their mouths leaking mercury, Hg, in intolerable amounts with open access to the brain. Their teeth contain up to 10 grams of Hg, while poisoning requires micrograms, only. Authorities do not worry about people getting sick, how to help them; some of their diseases are not even accepted. That experiment must be stopped and systematic restoration started.
While the results of fighting infectious diseases and of surgery are excellent, chronic diseases lag in spite of enormous efforts. They accelerate in both the old (1) and in the young generations, and innovative thinking is urgent. This paper deals with the problem of Amalgam in the correct way, different to that of the Establishment: To study the impact of Amalgams is to study Hg-chemistry. Logically it starts with the chemical and physical properties of Hg laid down by Nature, it uses Science of Nature and logical thinking to betray its attacks and its pathogenesis. It ends with methods of cure. This Science is unchangeable, non disputable, its validity is similar to that of e.g. the law of gravity. Thus man-made clinical results are wrong, when diverging. It calls the attention to the fact, that some of the claims of mercury being safe are based on scientific blunders. Conclusion: The claims of ADA are wrong.
Most of the chemistry of mercury, Hg, has been documented 100 years ago and needs no further documentation. It includes:
- Amalgam is claimed a stable alloy. No, it is highly unstable above the melting point of Hg, 39oC .
- It is a liquid with a significant vapour pressure. Air saturated with Hg holds about 50.000 µg/m3 at 37oC, 2.000 - 5.000 times the limit for working areas. Although the vapour pressure of amalgam is lower and the inhaled air does not get saturated, vapours from fillings have a terrible impact on a person, not 5 x 8, but 7 x 24 hours a week, life long from the first filling until its removal. Hg-vapours in the mouth are easily measured and made visible.
- All amalgam constituents corrode when more noble metals as gold, platinum or palladium are present in the same mouth. The electric element generated together with the saliva provides for that. The toxicity of more heavy metals is highly synergistic. Every pipe fitter knows not to mix different metals to avoid corrosion.
- All transition metals, able to exist in more valencies, generate a large number of free radicals, including the most powerful ones, the hydroxyl radicals. So does Hg.
- Hg shows an extreme affinity with sulphur containing compounds, most important are the amino acids cysteine and methionine placed in active centres of life important compounds and in proteins.
- Bacteria of the streptococcus family in plaque, i.e. in direct contact with the fillings, too, and in the GI-tract transform Hg to fat soluble methyl-Hg, MeHg, considered 100 times more toxic than Hg itself. This process is common to Nature from algae upwards and the reason, why marine animals are always contaminated with MeHg, not with elementary Hg.
- Amalgam is claimed a stable alloy. No, it is highly unstable above the melting point of Hg, 39oC .
- THE BEHAVIOUR OF MERCURY IN THE BODY.
- The release by vaporization and corrosion takes place from all visible and invisible surfaces, that are 3 - 5 times larger. There is sufficient room between the filling and the tooth to allow for the transport. It is increased by heat, acid liquids and the electric current generated by noble metals. Gold tendoubles the breakdown. Moreover wear adds heavily: Chewing, chewing gum, bruxism, tooth brushing, cleaning and polishing.
- Most Hg is released through the larger invisible surfaces via the teeth and jawbone directly into the blood. 20% of the vapour is expired, the rest is swallowed as is the corroded Hg. Metallic Hg is short-lived. It is either oxidized to Hg++ in blood or changed into MeHg. A minor portion of Hg-salts remain in the intestines for excretion, the urine carries what has been able to pass the kidneys. Hg++ attacks in 2 ways:
- Among the sources of free radicals, heavy metals are the only ones acting perpetually, and Hg from amalgam is by far the dominating source. It generates one radical/atom, often the most aggressive and most toxic hydroxyl type, which splits any substance hit. It recycles all the time: Hg++ --> Hg+ --> Hg++ a.s.o. The effect is increased multiple times and the person gets "oxidative stress".
- It is the metal fixing most avidly to sulphur in the SH-group of cysteine in DNA and other proteins; they may be deformed and lose their function. Also in enzymes, glutathione, one of our most potent antioxidants, in some hormones etc.
Tragedy No. 1: Cysteine is placed just in the active sites of enzymes etc. controlling our metabolism and all biological reactions in the body. Hg immobilizes them and their activity gets lost.
- We have no protection against MeHg. It penetrates cell membranes and barriers blood/brain, blood/retina, in the placenta and the mammary glands. It shows many destructive properties, i.a. a strong affinity for brain tissue and its ability of cell killing should be emphasized.
Tragedy No.2: The fetus/infant gets MeHg during the pregnancy and the nursing period and never more. It is the time of the formation of the brain and, if a girl, of her eggs. Just as bad: Hg in mothers ' blood concentrates in the umbilical cord and breast milk up to 8 times, as demonstrated by indisputable radioactive analyses. The small being gets Hg in proportion to the amount of blood and milk, but the damage is per unit of brainweight, so development is extremely affected during the first months of the pregnancy. It is evident that Hg blocking active sites in the fast cytogenesis of the brain will change or stop the process: The brain will be more or less incomplete. Ethyl-Hg ex thimerosal in vaccines behaves likewise. Its relation to autism has been made probable. The reagent contains 50%Hg, the same as amalgam, .
- The load on the population differs widely and two age groups are severely hit: The victims of the systematization in the 1930'es to 1960'es - now old age - got 12-14 fillings on average, in extreme cases 22 with up to 10 - 12 g Hg a few cm. below the brain with open access to it. Do dentists not learn anatomy? During the 1960'es protection against caries was successful. However, in the late 1970'es unstable high copper amalgam came into use, and the advantage of few fillings got lost. This type was preferred due to convenience and used in children, "it kills bacteria better". It was the most fatal and non controlled decision ever: The girls now transfer methyl-Hg to the brains of their children and the mental defects in the next generation and their escalation are explained.
Tragedy No. 3: All of it escalates contemporarily in both ends of the ages and the damage is going to remain during the new century if not counteracted now by rational means.
The final pollutants, Hg-cysteine and MeHg are extremely insoluble in our body liquids and our biological problem is that we have no means to get rid of them. The half times are very long, in the CNS > 25 years. Such a simple analysis as determining the rest of Hg in old fillings shows that half of Hg has disappeared in 10 -15 years, i.e. >1.000 µg/day. 3 grams are still in depots, i.e. > 100m. Hg-atoms in every single cell on average, mainly in the brain, the CNS, the pituitary, thyroid, other glands, kidneys, liver, lungs and heart. The immune system, sex cells, ovaries, testes and retina are also affected. Such a load suspending the actvity of vital substances controlling our health may interfere with all processes, and Hg ought to be hypothesis number one for any non explained disease.
- Among the sources of free radicals, heavy metals are the only ones acting perpetually, and Hg from amalgam is by far the dominating source. It generates one radical/atom, often the most aggressive and most toxic hydroxyl type, which splits any substance hit. It recycles all the time: Hg++ --> Hg+ --> Hg++ a.s.o. The effect is increased multiple times and the person gets "oxidative stress".
- The release by vaporization and corrosion takes place from all visible and invisible surfaces, that are 3 - 5 times larger. There is sufficient room between the filling and the tooth to allow for the transport. It is increased by heat, acid liquids and the electric current generated by noble metals. Gold tendoubles the breakdown. Moreover wear adds heavily: Chewing, chewing gum, bruxism, tooth brushing, cleaning and polishing.
- WHY DO DENTISTS NOT LEARN THESE BASICS TO KNOW WHAT THEY HAVE TO DO WITH?
I.a. because the teachers at the Universities are dentists, chemistry is not in vogue or its impact is not understood. Why have they forgotten the way of scientific thinking learned at Grammar school and used in this paper? Why has dentistry not studied Hg-chemistry before 1000's of tons were implanted two inches below the brain with open access through the olfactory bulb. Do dentists really trust that the mouth is the only spot, where Hg is safe, while it is supertoxic anywhere else. It speaks for itself.
Dentists are left in the lurch by this lack of education: While e.g. boring out old fillings, they inhale vapours and dust through the nose, that reach their brain as demonstrated by prof. Alfred Stock, Germany, in the 1930'es. Dentists show the highest rate of suicide in this country.
Often dentistry substantiates the safe claim on analyses of blood and urine, but these media are for transport, the pathogenic Hg has been fixed elsewhere. Claiming amalgam safe because
"Hg-levels are below values causing diseases", without considering the depots is a scientific blunder, and dental Science based on it is open to criticism or useless. Analyses of depots, e.g. part of the brain will not be available until post-mortem, unless biopsies are possible. Causal clinical trials are limited to the hypotheses looked for. Is Hg not included, the relationship will never be found. It may be due to professional policy, ignorance or no research money to this controversial topic. Such "science" has no sense.
Absence of proof is no proof of absence!
- GENERATED SYMPTOMS AND DISEASES.
Hg accumulates from the first filling and nervous tissue is the main target. When hurt some get ill insidiously, some at once. Some mental symptoms of this origin are well-known to poisoned patients and after replacement they disappear over the years. An incomplete list is:
Depression
anxiety
shyness
suicidal thoughts
headache
fatigue
tremor
muscle and joint pain
nervousness
vertigo
numbness
tingling of lips and fingers
irritability
visual disorders
lack of concentration
loss of memory
cold extremities.
frequent colds -> sinusitis
insomnia
loss of appetite -> loss of weight
increased blood pressure and cholesterol
heavy menstrual pains
This relationship appears to be unknown. The patients having these chronic disorders are not hypochondriacs, they are Hg-poisoned. Very often our papers are dealing with one or the other of these problems and the experts interviewed have no explanation.
- It is remarkable that highly qualified biochemical science has documented antioxidants to help chronically ill in general . The connection was confirmed in two JAMA-reviews (2)-(3) and (4). Thus the following diseases are mostly a consequence of "oxidative stress":.
senile dementia
Parkinson's and
Alzheimer's dz.
MS and ALS,
schizophrenia
fibromyalgia
epilepsy
migraine
tinnitus
chronic fatigue
atherosclerosis
cancer
osteoporosis
some rheumatic dz
some allergies:
asthma and psoriasis
cataract, AMD
other age-related eye diseases
reduced quality of sperm.
Bacterial resistance to Antibiotics due to Hg has been found. Several excellent investigations indicate a strong relation to Alzheimer's disease. An aorta from a by-pass operation had > 3.000 times, and a biopsy of a patient with idiopatic dilated cardiomyopathy showed 20.000 times the normal Hg-figure (5). How much is needed for a proof or a simple suspicion?
The mental retardation of many children, reduced IQ, demand for social assistance and special education, DAMP-children, autism, diabetes-2 at school age, hyperactivity, violence and criminality.
Dr. Hal Huggins, the US-dentist most experienced in correct amalgam replacement, reports to have cured i.a. leukemia, epilepsy, fibromyalgia, hypertension and hypercholesterolemia. Hypertension may appear as a result of Hg blocking some of the oxygen transport. The body creates more red blood cells to replace the capacity lost, viscosity increases and so does the pressure necessary for the circulation;
Summing up the numbers of patients suffering from the diseases above will show some 20% of the population. 80% seem genetically resistant, i.e. they do not feel worse, than they think it belongs to life. It is very urgent to find out why, because the tremendous number of people to be restored requires priorities. Some ideas of the genetic difference are at hand.
Hg is not claimed the only cause of chronic illness, but the major contributor. Thus many of these sufferings are man-made and per se superfluous. Our health depends on the power of attack and defence, and a disease develops depending just upon which part of the individual defence, that has been overrun.
More than half of the brain weight consists of lipids, many of which highly unsaturated and therefore specially susceptible to attack by free radicals. This is in line with the response of neurologic diseases to antioxidants. Add to this cysteine-destruction, cell killing MeHg. Damage of DNA by free-radical-splitting and Hg blocking its cysteine may lead to mutations, the first step on the way to cancer. A review on wildlife also tells of humans: Cromosome breakage, demyelination, dosedependent reductions in T-cell proliferation and constriction of the visual field. In mammals it concentrates selectively in the fetal brain, causes mental defects reduced fertility, fetal malformation and death (6). Is human Hg-chemistry different? Hardly.
The other amalgam metals, silver, copper and tin, are released due to corrosion and their chemistry and impact are similar, but less considered. They show strong synergy. Methyltin comes into existence similarly to MeHg. It is related to killing agents as TBT in boat paintings and is much more toxic.
Dentistry says: "During 150 years no diseases have been scientifically documented due to amalgam". This reasoning is baseless. A mistake is a mistake irrespective of age. It is correct to say: "For 150 years we have not understood the problem, but have unintentionally poisoned our patients incl. children having got Hg from their mothers". Universities are to blame. It has lead to an enormous waste of ressources: Wrong treatment and medication, hospitalization and operations, absence from work, too early ageing and retirement, misdirected medical research, neglected biochemical science a.s.o. The study reveals a majority of our most serious and costly health problems: Escalating amalgam toxicity occupies about half the expenditure of the health and care sectors. The Laws of Nature cover the whole area. Diseases of chemical origin are to be cured by removing the source and administering drop of chelating substances for the Hg++-compounds to be removed from depots, unfortunately only partly, and suitable sulphur and selenium containing supplements. So simple and yet a revolution.
About 1960 chemistry showed its relentless power, as thalidomide caused birth of 10.000 malformed children. The eternal and ubiquitous Laws of Physics and Chemistry controlling health, now show up again. The target is keeping people mentally alert and healthy until the end. The biochemists consider this a short time goal, see fig. Correct, provided the problem of Hg is tackled in the right way.
The off-hand change to the unstable type was a turning point. Now the young generation and their children are hit, so the problem will stay during the whole new century. It is the last minute to turn around, ban the poison and start the tremendous clean-up. The correct procedure must be used and learned. Some know how to do.
It will be an unpleasant decision, but the horror of to-day is self-inflicted.
- THE OFFICIAL DEFENCE FOR AMALGAM IS UNDER PRESSURE.
In response to my questions to the Danish government it admits: "Inorganic Hg is neurotoxic, organic Hg strongly neurotoxic causing extensive damages to the CNS and peripheral nerves. But these severe chronic toxicities cannot be compared to the minimal amounts released from fillings and stored in the organism".This reservation is not correct. In 1981 the controlling authority NIOM, Oslo, Norway, found the new high copper type to break down 50 times faster, releasing cadmium, too. The stability of amalgam became a disclosed lie. Since the late 70's it has been popular due to convenience. New guidelines in Norway advise against amalgam, because Hg was found in unwanted places: In the brains of dead people, in the fetus and in breast milk it correlates with the number of fillings of the mother. Acceptable composites exist for all teeth and purposes. The Danes say: There is a demonstrable relation between Hg in the fetus and infant and the number of fillings of the mother. Prof. Maths Berlin described his conclusions at the Congressional Hearings on May 8. Recently UNEP expressed very serious concerns on all uses of Hg including amalgam. In a short time the defence of amalgam is going to vanish and the authorities border on criminality when not stopping its use now.
Ref.
(1) Editorials. The global response to mental illness, BMJ, 2002; 325: 608-609.
(2) Fairfield KM, Fletcher RH, Harvard, Vitamins for Chronic Disease Prevention in Adults, Scientific Review, JAMA, 2002; 287: 3116-26. Covering 1966-Jan 11,2002, 152 ref.
(3) Fletcher RH, Fairfield KM, Ditto, Clinical Applications, ibid. 3127-29. 33 ref.
(4) Ames BN et al. High-dose vitamin therapy stimulates variant enzymes with .... relevance to genetic disease and polymorphisms. Am J Clin Nutr, 2002; 75: 616-58. 377 ref.
(5) Frustaci A et al. Marked Elevation of Myocardial Trace Elements in Idiopathic Dilated Cardiomyopathy Compared With Secondary Dysfunction. J Am Coll Cardiol. 1999; 33: 1578-1583.
(6) Wolfe MR et al. Effects of mercury on wildlife, a comprehensive review. Environ Toxic Chem 1998; 17: 146-60.
(7) Moller P. Mercury Amalgam: The Cause of Chronic Diseases, Mental Retardation in the Next Generation and Accelerated Aging. Clin Pract Altern Med, 2001; 2: 181-187. 44 ref.
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The Link Between Dental Fillings and Disease
Source: http://www.vimy-dentistry.com/nhanesgraphs.htm
NHANES III SCREENINGS – “THE WAY THINGS ARE”. NO B.S. STUDIES. THE TRUTH ABOUT
DENTAL FILLINGS AND DISEASE. COST: $120 MILLION DOLLARS TO COLLECT.
On graphs below: None = No Fillings, 1-7 = 1 Filling, 8-16 = 2-3 Fillings, 17-33 = 4-6 Fillings, 34-up = 7 or more Fillings
(Reason is filled surfaces were used. There are 128 filled surfaces, corresponding to all fillable 28 teeth, in the mouth)
Complete Chart Reference Guide
Below are all the charts done for the Amalgam Project, to show the differences in dental filling rates for the International Classification of Disease Codes. Here are the “signatures” that dental fillings leave for each disease. No two charts are alike, just as no two human beings are alike.
Dose-response relationships can be seen here, some diseases have upwards of 30% of survivors with more than 34 filled teeth surfaces (equivalent to 6 or more dental fillings), other diseases have a much higher rate of survivors being completely filling-free.
Because each disease is so unique in its dental fillings signature, we believe this to be a historic discovery. No more can it be said that dental fillings have “no effect” on disease. Clearly, they have a major effect. Otherwise, every chart would just have the shape of the solid line, which as you will see in a moment is the dental filling signature of the entire American Population.
ICD-9-CM Codes
How to read these graphs and charts:
a. The table in each section shows the Total U.S. Population of 180,072,328 people. Beside the “0”(zero) is the number of people, listed under “frequency”, who do NOT have the disease. Beside the “1”(one) is the number of people who DO have the disease, and are called“survivors”.
b. The graph in each section shows the dental filling distribution of the people who have the disease -“Yes”- in dotted line, and the rest of the population that does not have the disease -“No”- in solid line. The size of each group is the number in the table under “frequency” explained in (a) above.
c. The graph “x” axis then groups “filled surfaces” in 5 categories: None, 1-7, 8-16, 17-33, 34 up. To convert to filled teeth, there are 128 filled surfaces equating to 28 fillable teeth in a human being (8 incisors, 4 canines, 8 premolars and 8 molars). There are actually 32 teeth in the mouth, but Wisdom teeth are not filled, so are scored instead as present/absent and do not factor in this analysis. The conversion factor is roughly 4.6, so divide by 4.6 to convert filled surfaces to fillings. This is a more granular way of looking at teeth than dental fillings.
- Upper Left Central Incisor – 4 surfaces
- Upper Left Lateral Incisor – 4 surfaces
- Upper Left Cuspid – 4 surfaces
- Upper Left 1st Bicuspid – 5 surfaces
- Upper Left 2nd Bicuspid – 5 surfaces
- Upper Left 1st Molar – 5 surfaces
- Upper Left 2nd Molar – 5 surfaces
- Upper Left 3rd Molar – present/absent (wisdom tooth)
- Upper Right Central Incisor – 4 surfaces
- Upper Right Lateral Incisor – 4 surfaces
- Upper Right Cuspid – 4 surfaces
- Upper Right 1st Bicuspid – 5 surfaces
- Upper Right 2nd Bicuspid – 5 surfaces
- Upper Right 1st Molar – 5 surfaces
- Upper Right 2nd Molar – 5 surfaces
- Upper Right 3rd Molar – present/absent (wisdom tooth)
Same for Lower Right and Left Teeth. Total of 16 upper and 16 lower teeth, 32 teeth in all.
d. The higher the filled surfaces, the more dental fillings a patient has. The reason for these groupings is simple. Each grouping of filled surfaces is approximately 20% of the total U.S. Population of 180,072,328 people, the 5 groupings add up to 100%. We can then easily see by looking at disease groups how the dotted line (has the disease) varies from the solid line (does not have the disease). Most of the time, the solid line is nearly identical to the average U.S. population “norm” filling graph, so our attention is on the dotted line graph, which shows how groups that have the disease in question differ in dental filling distribution from average Americans.
e. Click on any hyperlink to get details of the Disease Code in that section. You will be connected via your web browser to Duke University.
1. Infectious and parasitic diseases (001-139)
We will show you how to read this section, it applies to all other sections. In the table, 2,182,813 Americans are living with Infectious and Parasitic Diseases at the time the NHANES III study was done. This is 1.2 Percent of the total American Population. The remaining 177,889,515 Americans do not have this disease. Looking at the graph, we see that 19% of survivors with this disease are filling-free (None), compared to 22% of the rest of Americans that are filling-free. So survivors of these diseases are filling-free more than the average American.
Also, they have higher rates of dental surface fillings in the 17-33 and 34-up categories, 24% vs 20% and 23% vs 19% respectively.
As we will see time and time again in this paper, dental fillings rates for disease groups do not look like the “average” rates for ordinary Americans. The larger the survivor group, the more filling-free they are, the smaller the survivor group the more fillings they have than average. It is disturbing, and the best way to lower your risk and/or increase your survival rate in either case is to be filling-free.
- intestinal infectious diseases (001-009)
- tuberculosis (010-018)
- zoonotic bacterial diseases (020-027)
- other bacterial diseases (030-041)
- human immunodeficiency virus (hiv) infection (042)
- poliomyelitis and other non-arthropod-borne viral diseases of central nervous system (045-049)
- viral diseases accompanied by exanthem (050-057)
- arthropod-borne viral diseases (060-066)
- other diseases due to viruses and chlamydiae (070-079)
- rickettsioses and other arthropod-borne diseases (080-088)
- syphilis and other venereal diseases (090-099)
- other spirochetal diseases (100-104)
- mycoses (110-118)
- helminthiases (120-129)
- other infectious and parasitic diseases (130-136)
- late effects of infectious and parasitic diseases (137-139)
2. Cancer [Neoplasms] (140-239)
Links to Cancer Mortality Rates
- malignant neoplasm of lip, oral cavity, and pharynx (140-149)
- malignant neoplasm of digestive organs and peritoneum (150-159)
- malignant neoplasm of respiratory and intrathoracic organs (160-165)
- malignant neoplasm of bone, connective tissue, skin, and breast (170-176)
- malignant neoplasm of genitourinary organs (179-189)
- malignant neoplasm of other and unspecified sites (190-199)
- benign neoplasms (210-229)
- carcinoma in situ (230-234)
- neoplasms of uncertain behavior (235-238)
- neoplasms of unspecified nature (239)
3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)
4. Diseases of the blood and blood-forming organs (280-289)
5. Mental disorders (290-319)
- psychoses (290-299)
- organic psychotic conditions (290-294)
- other psychoses (295-299)
- neurotic disorders, personality disorders, and other nonpsychotic mental disorders (300-316)
- mental retardation (317-319)
6. Diseases of the nervous system and sense organs (320-389)
7. Diseases of the circulatory system (390-459)
- acute rheumatic fever (390-392)
- chronic rheumatic heart disease (393-398)
- hypertensive disease (401-405)
- ischemic heart disease (410-414)
- diseases of pulmonary circulation (415-417)
- other forms of heart disease (420-429)
- cerebrovascular disease (430-438)
- diseases of arteries, arterioles, and capillaries (440-448)
- diseases of veins and lymphatics, and other diseases of circulatory system (451-459)
8. Diseases of the respiratory system (460-519)
- acute respiratory infections (460-466)
- other diseases of the upper respiratory tract (470-478)
- pneumonia and influenza (480-487)
- chronic obstructive pulmonary disease and allied conditions (490-496)
- pneumoconioses and other lung diseases due to external agents (500-508)
- other diseases of respiratory system (510-519)
9. Diseases of the digestive system (520-579)
- diseases of oral cavity, salivary glands, and jaws (520-529)
- diseases of esophagus, stomach, and duodenum (530-537)
- appendicitis (540-543)
- hernia of abdominal cavity (550-553)
- noninfectious enteritis and colitis (555-558)
- other diseases of intestines and peritoneum (560-569)
- other diseases of digestive system (570-579)
10. Diseases of the genitourinary system (580-629)
11. Complications of pregnancy, childbirth, and the puerperium (630-676)
- ectopic and molar pregnancy (630-633)
- other pregnancy with abortive outcome (634-639)
- complications mainly related to pregnancy (640-648)
- normal delivery, and other indications for care in pregnancy, labor, and delivery (650-659)
- complications occurring mainly in the course of labor and delivery (660-669)
- complications of the puerperium (670-676)
12. Diseases of the skin and subcutaneous tissue (680-709)
- infections of skin and subcutaneous tissue (680-686)
- other inflammatory conditions of skin and subcutaneous tissue (690-698)
- other diseases of skin and subcutaneous tissue (700-709)
13. Diseases of the musculoskeletal system and connective tissue (710-739)
- arthropathies and related disorders (710-719)
- dorsopathies (720-724)
- rheumatism, excluding the back (725-729)
- osteopathies, chondropathies, and acquired musculoskeletal deformities (730-739)
14. Congenital anomalies (740-759)
15. Certain conditions originating in the perinatal period (760-779)
- maternal causes of perinatal morbidity and mortality (760-763)
- other conditions originating in the perinatal period (764-779)
16. Symptoms, signs, and ill-defined conditions (780-799)
- symptoms (780-789)
- nonspecific abnormal findings (790-796)
- ill-defined and unknown causes of morbidity and mortality (797-799)
17. Injury and poisoning (800-999)
- fracture of skull (800-804)
- fracture of neck and trunk (805-809)
- fracture of upper limb (810-819)
- fracture of lower limb (820-829)
- dislocation (830-839)
- sprains and strains of joints and adjacent muscles (840-848)
- intracranial injury, excluding those with skull fracture (850-854)
- internal injury of thorax, abdomen, and pelvis (860-869)
- open wound (870-897)
- open wound of head, neck, and trunk (870-879)
- open wound of upper limb (880-887)
- open wound of lower limb (890-897)
- injury to blood vessels (900-904)
- late effects of injuries, poisonings, toxic effects, and other external causes (905-909)
- superficial injury (910-919)
- contusion with intact skin surface (920-924)
- crushing injury (925-929)
- effects of foreign body entering through orifice (930-939)
- burns (940-949)
- injury to nerves and spinal cord (950-957)
- certain traumatic complications and unspecified injuries (958-959)
- poisoning by drugs, medicinal and biological substances (960-979)
- toxic effects of substances chiefly nonmedicinal as to source (980-989)
- other and unspecified effects of external causes (990-995)
- complications of surgical and medical care, not elsewhere classified (996-999)
Supplementary classification of factors influencing health status and contact with health services (V01-V82)
- persons with potential health hazards related to communicable diseases (V01-V06)
- persons with potential health hazards related to personal and family history (V10-V19)
- persons encountering health services in circumstances related to reproduction and development (V20-V29)
- liveborn infants according to type of birth (V30-V39)
- persons with a condition influencing their health status (V40-V49)
- persons encountering health services for specific procedures and aftercare (V50-V59)
- persons encountering health services in other circumstances (V60-V68)
- persons without reported diagnosis encountered during examination and investigation of individuals and populations (V70-V82)
Source: http://www.vimy-dentistry.com/nhanesgraphs.htm
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