| PDX Collection 6211 (continued) |
| G40301 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40309 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40311 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40319 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40401 | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40409 | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40411 | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40419 | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G4042 | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
| G40501 | Epileptic seizures related to external causes, not intractable, with status epilepticus |
| G40509 | Epileptic seizures related to external causes, not intractable, without status epilepticus |
| G40801 | Other epilepsy, not intractable, with status epilepticus |
| G40802 | Other epilepsy, not intractable, without status epilepticus |
| G40803 | Other epilepsy, intractable, with status epilepticus |
| G40804 | Other epilepsy, intractable, without status epilepticus |
| G40811 | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
| G40812 | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
| G40813 | Lennox-Gastaut syndrome, intractable, with status epilepticus |
| G40814 | Lennox-Gastaut syndrome, intractable, without status epilepticus |
| G40821 | Epileptic spasms, not intractable, with status epilepticus |
| G40822 | Epileptic spasms, not intractable, without status epilepticus |
| G40823 | Epileptic spasms, intractable, with status epilepticus |
| G40824 | Epileptic spasms, intractable, without status epilepticus |
| G40833 | Dravet syndrome, intractable, with status epilepticus |
| G40834 | Dravet syndrome, intractable, without status epilepticus |
| G4089 | Other seizures |
| G40901 | Epilepsy, unspecified, not intractable, with status epilepticus |
| G40909 | Epilepsy, unspecified, not intractable, without status epilepticus |
| G40911 | Epilepsy, unspecified, intractable, with status epilepticus |
| G40919 | Epilepsy, unspecified, intractable, without status epilepticus |
| G40A01 | Absence epileptic syndrome, not intractable, with status epilepticus |
| G40A09 | Absence epileptic syndrome, not intractable, without status epilepticus |
| G40A11 | Absence epileptic syndrome, intractable, with status epilepticus |
| G40A19 | Absence epileptic syndrome, intractable, without status epilepticus |
| G40B01 | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
| G40B09 | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
| G40B11 | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
| G40B19 | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
| G40C01 | Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus |
| G40C09 | Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus |
| G40C11 | Lafora progressive myoclonus epilepsy, intractable, with status epilepticus |
| G40C19 | Lafora progressive myoclonus epilepsy, intractable, without status epilepticus |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| R561 | Post traumatic seizures |
| |
| PDX Collection 6212 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8984 | IgG4-related disease |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 6213 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8984 | IgG4-related disease |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 6214 |
| I200 | Unstable angina |
| I201 | Angina pectoris with documented spasm |
| I202 | Refractory angina pectoris |
| I2081 | Angina pectoris with coronary microvascular dysfunction |
| I2089 | Other forms of angina pectoris |
| I209 | Angina pectoris, unspecified |
| I2101 | ST elevation (STEMI) myocardial infarction involving left main coronary artery |
| I2102 | ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery |
| I2109 | ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall |
| I2111 | ST elevation (STEMI) myocardial infarction involving right coronary artery |
| I2119 | ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall |
| I2121 | ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery |
| I2129 | ST elevation (STEMI) myocardial infarction involving other sites |
| I213 | ST elevation (STEMI) myocardial infarction of unspecified site |
| I214 | Non-ST elevation (NSTEMI) myocardial infarction |
| I219 | Acute myocardial infarction, unspecified |
| I21A1 | Myocardial infarction type 2 |
| I21A9 | Other myocardial infarction type |
| I21B | Myocardial infarction with coronary microvascular dysfunction |
| I220 | Subsequent ST elevation (STEMI) myocardial infarction of anterior wall |
| I221 | Subsequent ST elevation (STEMI) myocardial infarction of inferior wall |
| I222 | Subsequent non-ST elevation (NSTEMI) myocardial infarction |
| I228 | Subsequent ST elevation (STEMI) myocardial infarction of other sites |
| I229 | Subsequent ST elevation (STEMI) myocardial infarction of unspecified site |
| I240 | Acute coronary thrombosis not resulting in myocardial infarction |
| I241 | Dressler's syndrome |
| I2481 | Acute coronary microvascular dysfunction |
| I2489 | Other forms of acute ischemic heart disease |
| I249 | Acute ischemic heart disease, unspecified |
| I255 | Ischemic cardiomyopathy |
| I256 | Silent myocardial ischemia |
| I25702 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with refractory angina pectoris |
| I25712 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with refractory angina pectoris |
| I25722 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with refractory angina pectoris |
| I25732 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with refractory angina pectoris |
| I25752 | Atherosclerosis of native coronary artery of transplanted heart with refractory angina pectoris |
| I25762 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory angina pectoris |
| I25792 | Atherosclerosis of other coronary artery bypass graft(s) with refractory angina pectoris |
| I2585 | Chronic coronary microvascular dysfunction |
| I2589 | Other forms of chronic ischemic heart disease |
| I259 | Chronic ischemic heart disease, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| |
| PDX Collection 6215 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8984 | IgG4-related disease |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 6216 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8984 | IgG4-related disease |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 6217 |
| I440 | Atrioventricular block, first degree |
| I441 | Atrioventricular block, second degree |
| I442 | Atrioventricular block, complete |
| I4430 | Unspecified atrioventricular block |
| I4439 | Other atrioventricular block |
| I444 | Left anterior fascicular block |
| I445 | Left posterior fascicular block |
| I4460 | Unspecified fascicular block |
| I4469 | Other fascicular block |
| I447 | Left bundle-branch block, unspecified |
| I450 | Right fascicular block |
| I4510 | Unspecified right bundle-branch block |
| I4519 | Other right bundle-branch block |
| I452 | Bifascicular block |
| I453 | Trifascicular block |
| I454 | Nonspecific intraventricular block |
| I455 | Other specified heart block |
| I456 | Pre-excitation syndrome |
| I4581 | Long QT syndrome |
| I4589 | Other specified conduction disorders |
| I459 | Conduction disorder, unspecified |
| I469 | Cardiac arrest, cause unspecified |
| I470 | Re-entry ventricular arrhythmia |
| I4710 | Supraventricular tachycardia, unspecified |
| I4711 | Inappropriate sinus tachycardia, so stated |
| I4719 | Other supraventricular tachycardia |
| I4720 | Ventricular tachycardia, unspecified |
| I4721 | Torsades de pointes |
| I4729 | Other ventricular tachycardia |
| I479 | Paroxysmal tachycardia, unspecified |
| I480 | Paroxysmal atrial fibrillation |
| I4811 | Longstanding persistent atrial fibrillation |
| I4819 | Other persistent atrial fibrillation |
| I4820 | Chronic atrial fibrillation, unspecified |
| I4821 | Permanent atrial fibrillation |
| I483 | Typical atrial flutter |
| I484 | Atypical atrial flutter |
| I4891 | Unspecified atrial fibrillation |
| I4892 | Unspecified atrial flutter |
| I4901 | Ventricular fibrillation |
| I4902 | Ventricular flutter |
| I492 | Junctional premature depolarization |
| I498 | Other specified cardiac arrhythmias |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| R001 | Bradycardia, unspecified |
| |
| PDX Collection 6218 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8984 | IgG4-related disease |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 6219 |
| I240 | Acute coronary thrombosis not resulting in myocardial infarction |
| I241 | Dressler's syndrome |
| I2481 | Acute coronary microvascular dysfunction |
| I2489 | Other forms of acute ischemic heart disease |
| I249 | Acute ischemic heart disease, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| |
| PDX Collection 6220 |
| I440 | Atrioventricular block, first degree |
| I441 | Atrioventricular block, second degree |
| I442 | Atrioventricular block, complete |
| I4430 | Unspecified atrioventricular block |
| I4439 | Other atrioventricular block |
| I444 | Left anterior fascicular block |
| I445 | Left posterior fascicular block |
| I4460 | Unspecified fascicular block |
| I4469 | Other fascicular block |
| I447 | Left bundle-branch block, unspecified |
| I450 | Right fascicular block |
| I4510 | Unspecified right bundle-branch block |
| I4519 | Other right bundle-branch block |
| I452 | Bifascicular block |
| I453 | Trifascicular block |
| I454 | Nonspecific intraventricular block |
| I455 | Other specified heart block |
| I456 | Pre-excitation syndrome |
| I4581 | Long QT syndrome |
| I4589 | Other specified conduction disorders |
| I459 | Conduction disorder, unspecified |
| I469 | Cardiac arrest, cause unspecified |
| I470 | Re-entry ventricular arrhythmia |
| I4710 | Supraventricular tachycardia, unspecified |
| I4711 | Inappropriate sinus tachycardia, so stated |
| I4719 | Other supraventricular tachycardia |
| I4720 | Ventricular tachycardia, unspecified |
| I4721 | Torsades de pointes |
| I4729 | Other ventricular tachycardia |
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