ICD-10 Chapter IX: Diseases of the circulatory system
I00-I99 – Diseases of the circulatory system
I00-I99 – Diseases of the circulatory system
(I00-I02) Acute rheumatic fever
- (I00) Rheumatic fever without mention of heart involvement
- (I01) Rheumatic fever with heart involvement
- (I01.0) Acute rheumatic pericarditis
- (I01.1) Acute rheumatic endocarditis
- (I01.2) Acute rheumatic myocarditis
- (I01.8) Other acute rheumatic heart disease
- (I01.9) Acute rheumatic heart disease, unspecified
(I05-I09) Chronic rheumatic heart diseases
- (I05) Rheumatic mitral valve diseases
- (I06) Rheumatic aortic valve diseases
- (I07) Rheumatic tricuspid valve diseases
- (I08) Multiple valve diseases
- (I08.0) Disorders of both mitral and aortic valves
- (I08.1) Disorders of both mitral and tricuspid valves
- (I08.2) Disorders of both aortic and tricuspid valves
- (I08.3) Combined disorders of mitral, aortic and tricuspid valves
- (I09) Other rheumatic heart diseases
- (I09.0) Rheumatic myocarditis
- (I09.1) Rheumatic diseases of endocardium, valve unspecified
- (I09.2) Chronic rheumatic pericarditis
- (I09.9) Rheumatic heart disease, unspecified
(I10-I15) Hypertensive diseases
- (I10) Essential (primary) hypertension
- (I11) Hypertensive heart disease
- (I12) Hypertensive renal disease
- (I13) Hypertensive heart disease and Hypertensive renal disease
- (I15) Secondary hypertension
(I20-I25) Ischemic heart diseases
- (I20) Angina pectoris
- (I20.0) Unstable angina
- (I20.1) Angina pectoris with documented spasm
- (I20.8) Other forms of angina pectoris
- (I20.9) Angina pectoris, unspecified
- (I22) Subsequent myocardial infarction
- (I23) Certain current complications following acute myocardial infarction
- (I23.0) Haemopericardium as current complication following acute myocardial infarction
- (I23.1) Atrial septal defect as current complication following acute myocardial infarction
- (I23.2) Ventricular septal defect as current complication following acute myocardial infarction
- (I23.3) Rupture of cardiac wall without haemopericardium as current complication following acute myocardial infarction
- (I23.4) Rupture of chordae tendineae as current complication following acute myocardial infarction
- (I23.5) Rupture of papillary muscle as current complication following acute myocardial infarction
- (I23.6) Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
- (I23.8) Other current complications following acute myocardial infarction
- (I24) Other acute ischaemic heart diseases
- (I24.0) Coronary thrombosis not resulting in myocardial infarction
- (I24.1) Dressler’s syndrome
- (I25) Chronic ischaemic heart disease
- (I25.0) Atherosclerotic cardiovascular disease, so described
- (I25.1) Atherosclerotic heart disease
- (I25.2) Old myocardial infarction
- (I25.3) Aneurysm of heart
- (I25.4) Coronary artery aneurysm
- (I25.5) Ischaemic cardiomyopathy
- (I25.6) Silent myocardial ischaemia
- (I25.8) Other forms of chronic ischaemic heart disease
- (I25.9) Chronic ischaemic heart disease, unspecified
(I26-I28) Pulmonary heart disease and diseases of pulmonary circulation
- (I26) Pulmonary embolism
- (I27) Other pulmonary heart diseases
- (I27.0) Primary pulmonary hypertension
- (I27.1) Kyphoscoliotic heart disease
- (I27.2) Other secondary pulmonary hypertension
- (I27.8) Other specified pulmonary heart diseases
- (I27.9) Pulmonary heart disease, unspecified
- (I28) Other diseases of pulmonary vessels
- (I28.0) Arteriovenous fistula of pulmonary vessels
- (I28.1) Aneurysm of pulmonary artery
- (I28.8) Other specified diseases of pulmonary vessels
- (I28.9) Disease of pulmonary vessels, unspecified
(I30-I52) Other forms of heart disease
- (I30) Acute pericarditis
- (I31) Other diseases of pericardium
- (I31.0) Chronic adhesive pericarditis
- (I31.1) Chronic constrictive pericarditis
- (I31.2) Haemopericardium, not elsewhere classified
- (I31.3) Pericardial effusion (noninflammatory)
- (I31.8) Other specified diseases of pericardium
- (I31.9) Disease of pericardium, unspecified
- (I32) Pericarditis in diseases classified elsewhere
endocardium (including heart valves)
- (I33) Acute and subacute endocarditis
- (I34) Nonrheumatic mitral valve disorders
- (I35) Nonrheumatic aortic valve disorders
- (I36) Nonrheumatic tricuspid valve disorders
- (I36.0) Nonrheumatic tricuspid (valve) stenosis
- (I36.1) Nonrheumatic tricuspid (valve) insufficiency
- (I36.2) Nonrheumatic tricuspid (valve) stenosis with insufficiency
- (I37) Pulmonary valve disorders
- (I38) Endocarditis, valve unspecified
- (I39) Endocarditis and heart valve disorders in diseases classified elsewhere
- (I41) Myocarditis in diseases classified elsewhere
- (I42) Cardiomyopathy
- (I42.0) Dilated cardiomyopathy
- (I42.1) Obstructive hypertrophic cardiomyopathy
- (I42.2) Other hypertrophic cardiomyopathy
- (I42.3) Endomyocardial (eosinophilic) disease
- (I42.4) Endocardial fibroelastosis
- (I42.5) Other restrictive cardiomyopathy
- (I42.6) Alcoholic cardiomyopathy
- (I42.8) Other cardiomyopathies
- (I43) Cardiomyopathy in diseases classified elsewhere
- (I44) Atrioventricular and left bundle-branch block
- (I44.0) Atrioventricular block, first degree
- (I44.1) Atrioventricular block, second degree
- (I44.2) Atrioventricular block, complete
- (I44.3) Other and unspecified atrioventricular block
- (I44.4) Left anterior fascicular block
- (I44.5) Left posterior fascicular block
- (I44.6) Other and unspecified fascicular block
- (I44.7) Left bundle-branch block, unspecified
- (I45) Other conduction disorders
- (I45.0) Right fascicular block
- (I45.1) Other and unspecified right bundle-branch block
- (I45.2) Bifascicular block
- (I45.3) Trifascicular block
- (I45.4) Nonspecific intraventricular block
- (I45.5) Other specified heart block
- (I45.6) Pre-excitation syndrome
- (I45.8) Other specified conduction disorders
- (I45.9) Conduction disorder, unspecified
- (I46) Cardiac arrest
- (I46.0) Cardiac arrest with successful resuscitation
- (I46.1) Sudden cardiac death, so described
- (I46.9) Cardiac arrest, unspecified
- (I48) Atrial fibrillation and flutter
- (I49) Other cardiac arrhythmias
- (I49.0) Ventricular fibrillation and flutter
- (I49.1) Atrial premature depolarization
- (I49.2) Junctional premature depolarization
- (I49.3) Ventricular premature depolarization
- (I49.4) Other and unspecified premature depolarization
- (I49.5) Sick sinus syndrome
- (I49.8) Other specified cardiac arrhythmias
- (I49.9) Cardiac arrhythmia, unspecified
other
- (I51) Complications and ill-defined descriptions of heart disease
- (I51.4) Myocarditis, unspecified
- (I51.6) Cardiovascular disease, unspecified
- (I51.7) Cardiomegaly
- (I52) Other heart disorders in diseases classified elsewhere
(I60-I69) Cerebrovascular diseases
- (I60.0) Subarachnoid haemorrhage from carotid siphon and bifurcation
- (I60.1) Subarachnoid haemorrhage from middle cerebral artery
- (I60.2) Subarachnoid haemorrhage from anterior communicating artery
- (I60.3) Subarachnoid haemorrhage from posterior communicating artery
- (I60.4) Subarachnoid haemorrhage from basilar artery
- (I60.5) Subarachnoid haemorrhage from vertebral artery
- (I60.6) Subarachnoid haemorrhage from other intracranial arteries
- (I60.7) Subarachnoid haemorrhage from intracranial artery, unspecified
- (I61) Intracerebral haemorrhage
- (I61.0) Intracerebral haemorrhage in hemisphere, subcortical
- (I61.1) Intracerebral haemorrhage in hemisphere, cortical
- (I61.2) Intracerebral haemorrhage in hemisphere, unspecified
- (I61.3) Intracerebral haemorrhage in brain stem
- (I61.4) Intracerebral haemorrhage in cerebellum
- (I61.5) Intracerebral haemorrhage, intraventricular
- (I61.6) Intracerebral haemorrhage, multiple localized
- (I62) Other nontraumatic intracranial haemorrhage
- (I62.0) Subdural haemorrhage (acute)(nontraumatic)
- (I62.1) Nontraumatic extradural haemorrhage
- Nontraumatic epidural haemorrhage
- (I63) Cerebral infarction
- (I63.0) Cerebral infarction due to thrombosis of precerebral arteries
- (I63.1) Cerebral infarction due to embolism of precerebral arteries
- (I63.2) Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries
- (I63.3) Cerebral infarction due to thrombosis of cerebral arteries
- (I63.4) Cerebral infarction due to embolism of cerebral arteries
- (I63.5) Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries
- (I63.6) Cerebral infarction due to cerebral venous thrombosis, nonpyogenic
- (I64) Stroke, not specified as hemorrhage or infarction
- (I65) Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction
- (I65.0) Occlusion and stenosis of vertebral artery
- (I65.1) Occlusion and stenosis of basilar artery
- (I65.2) Occlusion and stenosis of carotid artery
- (I65.3) Occlusion and stenosis of multiple and bilateral precerebral arteries
- (I65.8) Occlusion and stenosis of other precerebral artery
- (I65.9) Occlusion and stenosis of unspecified precerebral artery
- (I66) Occlusion and stenosis of cerebral arteries, not resulting in cerebral infarction
- (I66.0) Occlusion and stenosis of middle cerebral artery
- (I66.1) Occlusion and stenosis of anterior cerebral artery
- (I66.2) Occlusion and stenosis of posterior cerebral artery
- (I66.3) Occlusion and stenosis of cerebellar arteries
- (I66.4) Occlusion and stenosis of multiple and bilateral cerebral arteries
- (I66.5) Occlusion and stenosis of other cerebral artery
- (I66.6) Occlusion and stenosis of unspecified cerebral artery
- (I67) Other cerebrovascular diseases
- (I67.1) Cerebral aneurysm, nonruptured
- (I67.2) Cerebral atherosclerosis
- (I67.3) Progressive vascular leukoencephalopathy
- (I67.4) Hypertensive encephalopathy
- (I67.5) Moyamoya disease
- (I67.6) Nonpyogenic thrombosis of intracranial venous system
- (I67.7) Cerebral arteritis, not elsewhere classified
- (I68) Cerebrovascular disorders in diseases classified elsewhere
(I70-I79) Diseases of arteries, arterioles and capillaries
- (I71) Aortic aneurysm and dissection
- (I71.0) Dissection of aorta (any part)
- (I71.1) Thoracic aortic aneurysm, ruptured
- (I71.2) Thoracic aortic aneurysm, without mention of rupture
- (I71.3) Abdominal aortic aneurysm, ruptured
- (I71.4) Abdominal aortic aneurysm, without mention of rupture
- (I71.5) Thoracoabdominal aortic aneurysm, ruptured
- (I71.6) Thoracoabdominal aortic aneurysm, without mention of rupture
- (I71.8) Aortic aneurysm of unspecified site, ruptured
- (I71.9) Aortic aneurysm of unspecified site, without mention of rupture
- (I73) Other peripheral vascular diseases
- (I73.0) Raynaud’s syndrome
- (I73.1) Thromboangiitis obliterans (Buerger)
- (I73.8) Other specified peripheral vascular diseases
- (I73.9) Peripheral vascular disease, unspecified
- (I74) Arterial embolism and thrombosis
- (I77) Other disorders of arteries and arterioles
- (I77.0) Arteriovenous fistula, acquired
- (I77.1) Stricture of artery
- (I77.2) Rupture of artery
- (I77.3) Arterial fibromuscular dysplasia
- (I77.4) Coeliac artery compression syndrome
- (I77.5) Necrosis of artery
- (I77.6) Arteritis, unspecified
- (I77.8) Other specified disorders of arteries and arterioles
- (I77.9) Disorder of arteries and arterioles, unspecified
- (I78) Diseases of capillaries
- (I78.0) Hereditary haemorrhagic telangiectasia
- (I78.1) Naevus, non-neoplastic
- (I78.8) Other diseases of capillaries
- (I78.9) Disease of capillaries, unspecified
- (I79) Disorders of arteries, arterioles and capillaries in diseases classified elsewhere
(I80-I89) Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified
- (I80) Phlebitis and thrombophlebitis
- (I80.0) Phlebitis and thrombophlebitis of superficial vessels of lower extremities
- (I80.1) Phlebitis and thrombophlebitis of femoral vein
- (I80.2) Phlebitis and thrombophlebitis of other deep vessels of lower extremities
- (I82) Other venous embolism and venous thrombosis
- (I82.0) Budd-Chiari syndrome
- (I82.1) Thrombophlebitis migrans
- (I82.2) Embolism and thrombosis of vena cava
- (I82.3) Embolism and thrombosis of renal vein
- (I82.8) Embolism and thrombosis of other specified veins
- (I84) Haemorrhoids
- (I84.6) Residual haemorrhoidal skin tags
- (I86) Varicose veins of other sites
- (I86.0) Sublingual varices
- (I86.1) Scrotal varices
- (I86.2) Pelvic varices
- (I86.3) Vulval varices
- (I86.4) Gastric varices
- (I86.8) Varicose veins of other specified sites
- (I87) Other disorders of veins
- (I87.0) Postphlebitic syndrome
- (I87.1) Compression of vein
- (I87.2) Venous insufficiency (chronic)(peripheral)
- (I87.8) Other specified disorders of veins
- (I87.9) Disorder of vein, unspecified
- (I88) Nonspecific lymphadenitis
- (I89) Other noninfective disorders of lymphatic vessels and lymph nodes
- (I89.0) Lymphoedema, not elsewhere classified
- (I89.1) Lymphangitis
- (I89.8) Other specified noninfective disorders of lymphatic vessels and lymph nodes
- (I89.9) Noninfective disorder of lymphatic vessels and lymph nodes, unspecified
(I95-I99) Other and unspecified disorders of the circulatory system
- (I95) Hypotension
- (I95.0) Idiopathic hypotension
- (I95.1) Orthostatic hypotension
- (I95.2) Hypotension due to drugs
- (I95.9) Hypotension, unspecified
- (I97) Postprocedural disorders of circulatory system, not elsewhere classified
- (I98) Other disorders of circulatory system in diseases classified elsewhere
- (I99) Other and unspecified disorders of circulatory system
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview

The circulatory system is an organ system that moves nutrients, gases, and wastes to and from cells, helps fight diseases and helps stabilize body temperature and pH to maintain homeostasis. This system may be seen strictly as a blood distribution network, but some consider the circulatory system as composed of the cardiovascular system, which distributes blood, and the lymphatic system, which distributes lymph. While humans, as well as other vertebrates, have a closed cardiovascular system (meaning that the blood never leaves the network of arteries, veins and capillaries), some invertebrate groups have an open cardiovascular system. The most primitive animal phyla lack circulatory systems. The lymphatic system, on the other hand, is an open system.
Human circulatory system
The main components of the human circulatory system are the heart, the blood, and the blood vessels. The circulatory system includes: the pulmonary circulation, a “loop” through the lungs where blood is oxygenated; and the systemic circulation, a “loop” through the rest of the body to provide oxygenated blood. An average adult contains five to six quarts (roughly 4.7 to 5.7 liters) of blood, which consists of plasma that contains red blood cells, white blood cells, and platelets.
Two types of fluids move through the circulatory system: blood and lymph. The blood, heart, and blood vessels form the cardiovascular system. The lymph, lymph nodes, and lymph vessels form the lymphatic system. The cardiovascular system and the lymphatic system collectively make up the circulatory system.
Systemic circulation
Systemic circulation is the portion of the cardiovascular system which carries oxygenated blood away from the heart, to the body, and returns deoxygenated blood back to the heart.
Arteries always take blood away from the heart, regardless of their oxygenation, and veins always bring blood back. In general, arteries bring oxygenated blood to the tissues; veins bring deoxygenated blood back to the heart. In the case of the pulmonary vessels, however, the oxygenation is reversed: the pulmonary artery takes deoxygenated blood from the heart to the lungs, and oxygenated blood is pumped back through the pulmonary vein to the heart. As blood circulates through the body, oxygen and nutrients diffuse from the blood into cells surrounding the capillaries, and carbon dioxide diffuses into the blood from the capillary cells.[1]
The release of oxygen from red blood cells or erythrocytes is regulated in mammals. It increases with an increase of carbon dioxide in tissues, an increase in temperature, or a decrease in pH. Such characteristics are exhibited by tissues undergoing high metabolism, as they require increased levels of oxygen.
Pulmonary circulation
Pulmonary circulation is the portion of the cardiovascular system which carries oxygen-depleted blood away from the heart, to the lungs, and returns oxygenated blood back to the heart.
De-oxygenated blood enters the right atrium of the heart and flows into the right ventricle where it is pumped through the pulmonary arteries to the lungs. Pulmonary veins return the now oxygen-rich blood to the heart, where it enters the left atrium before flowing into the left ventricle. From the left ventricle the oxygen-rich blood is pumped out via the aorta, and on to the rest of the body.
Coronary circulation
The coronary circulatory system provides a blood supply to the heart.
Heart
In the heart there is one atrium and one ventricle for each circulation, and with both a systemic and a pulmonary circulation there are four chambers in total: left atrium, left ventricle, right atrium and right ventricle.
Closed cardiovascular system
The cardiovascular systems of humans is closed, meaning that the blood never leaves the system of blood vessels. In contrast, oxygen and nutrients diffuse across the blood vessel layers and enters interstitial fluid, which carries oxygen and nutrients to the target cells, and carbon dioxide and wastes in the opposite direction. The other component of the circulatory system, the lymphatic system, is not closed.
Other vertebrates
The circulatory systems of all vertebrates, as well as of annelids (for example, earthworms) and cephalopods (squid and octopus) are closed, just as in humans. Still, the systems of fish, amphibians, reptiles, and birds show various stages of the evolution of the circulatory system.
In fish, the system has only one circuit, with the blood being pumped through the capillaries of the gills and on to the capillaries of the body tissues. This is known as single circulation. The heart of fish is therefore only a single pump (consisting of two chambers). In amphibians and most reptiles, a double circulatory system is used, but the heart is not always completely separated into two pumps. Amphibians have a three-chambered heart.
Birds and mammals show complete separation of the heart into two pumps, for a total of four heart chambers; it is thought that the four-chambered heart of birds evolved independently from that of mammals.
Open circulatory system
The open circulatory system is an arrangement of internal transport present in many animals such as molluscs and arthropods, in which fluid (called hemolymph) in a cavity called the hemocoel bathes the organs directly with oxygen and nutrients and there is no distinction between blood and interstitial fluid; this combined fluid is called hemolymph or haemolymph. Muscular movements by the animal during locomotion can facilitate hemolymph movement, but diverting flow from one area to another is limited. When the heart relaxes, blood is drawn back toward the heart through open-ended pores (ostia).
Hemolymph fills all of the interior hemocoel of the body and surrounds all cells. Hemolymph is composed of water, inorganic salts (mostly Na+, Cl–, K+, Mg2+, and Ca2+), and organic compounds (mostly carbohydrates, proteins, and lipids). The primary oxygen transporter molecule is hemocyanin.
There are free-floating cells, the hemocytes, within the hemolymph. They play a role in the arthropod immune system.
No circulatory system
Circulatory systems are absent in some animals, including flatworms (phylum Platyhelminthes). Their body cavity has no lining or enclosed fluid. Instead a muscular pharynx leads to an extensively branched digestive system that facilitates direct diffusion of nutrients to all cells. The flatworm’s dorso-ventrally flattened body shape also restricts the distance of any cell from the digestive system or the exterior of the organism. Oxygen can diffuse from the surrounding water into the cells, and carbon dioxide can diffuse out. Consequently every cell is able to obtain nutrients, water and oxygen without the need of a transport system.
Measurement techniques
- Electrocardiogram — for cardiac electrophysiology
- Sphygmomanometer and stethoscope — for blood pressure
- Pulse meter — for cardiac function (heart rate, rhythm, dropped beats)
- Pulse — commonly used to determine the heart rate in absence of certain cardiac pathologies
- Nail bed blanching test — test for perfusion
- Vessel cannula or catheter pressure measurement — pulmonary wedge pressure or in older animal experiments.
Health and disease
History of discovery
The valves of the heart were discovered by a physician of the Hippocratean school around the 4th century BC. However their function was not properly understood then. Because blood pools in the veins after death, arteries look empty. Ancient anatomists assumed they were filled with air and that they were for transport of air.
Herophilus distinguished veins from arteries but thought that the pulse was a property of arteries themselves. Erasistratus observed that arteries that were cut during life bleed. He ascribed the fact to the phenomenon that air escaping from an artery is replaced with blood that entered by very small vessels between veins and arteries. Thus he apparently postulated capillaries but with reversed flow of blood.
The 2nd century AD, Greek physician, Galen, knew that blood vessels carried blood and identified venous (dark red) and arterial (brighter and thinner) blood, each with distinct and separate functions. Growth and energy were derived from venous blood created in the liver from chyle, while arterial blood gave vitality by containing pneuma (air) and originated in the heart. Blood flowed from both creating organs to all parts of the body where it was consumed and there was no return of blood to the heart or liver. The heart did not pump blood around, the heart’s motion sucked blood in during diastole and the blood moved by the pulsation of the arteries themselves.
Galen believed that the arterial blood was created by venous blood passing from the left ventricle to the right by passing through ‘pores’ in the interventricular septum, air passed from the lungs via the pulmonary artery to the left side of the heart. As the arterial blood was created ‘sooty’ vapors were created and passed to the lungs also via the pulmonary artery to be exhaled.
In 1242, the Arabian physician, Ibn al-Nafis, became the first person to accurately describe the process of blood circulation in the human body, particularly pulmonary circulation, for which he is considered the father of circulatory physiology.[2] Ibn al-Nafis stated in his Commentary on Anatomy in Avicenna’s Canon:
“…the blood from the right chamber of the heart must arrive at the left chamber but there is no direct pathway between them. The thick septum of the heart is not perforated and does not have visible pores as some people thought or invisible pores as Galen thought. The blood from the right chamber must flow through the vena arteriosa (pulmonary artery) to the lungs, spread through its substances, be mingled there with air, pass through the arteria venosa (pulmonary vein) to reach the left chamber of the heart and there form the vital spirit…”
Contemporary drawings of this process have survived. In 1552, Michael Servetus described the same, and Realdo Colombo proved the concept, but it remained largely unknown in Europe.
Finally William Harvey, a pupil of Hieronymus Fabricius (who had earlier described the valves of the veins without recognizing their function), performed a sequence of experiments and announced in 1628 the discovery of the human circulatory system as his own and published an influential book about it. This work with its essentially correct exposition slowly convinced the medical world. Harvey was not able to identify the capillary system connecting arteries and veins; these were later described by Marcello Malpighi.
Video: Examination of Cardiovascular System
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See also
References
- ↑ Maton, Anthea (1993). Human Biology and Health. Englewood Cliffs, New Jersey: Prentice Hall. ISBN 0-13-981176-1. Unknown parameter
|coauthors=ignored (help) - ↑ Chairman’s Reflections (2004), “Traditional Medicine Among Gulf Arabs, Part II: Blood-letting”, Heart Views 5 (2), p. 74-85 [80].
External links
- The Circulatory System, a comprehensive overview
- The InVision Guide to a Healthy Heart An interactive website
- NCP Cardiovascular Medicine A Journal Covering Clinical Cardiovascular Medicine
Template:Development of circulatory system
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See also
See also
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- List of ICD-9 codes 390-459: Diseases of the circulatory system
hu:BNO-10-09 – A keringési rendszer betegségei nl:ICD10 Hoofdstuk IX te:ICD-10 అధ్యాయము 9: రక్తప్రసరణ వ్యవస్థ సంబంధిత వ్యాధులు th:ICD-10 บท I: โรคระบบไหลเวียนโลหิต
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