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ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
Page 1162 of 1375 |
PDX Collection 6212 (continued) | |
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 |
D8481 | Immunodeficiency due to conditions classified elsewhere |
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 |
D8481 | Immunodeficiency due to conditions classified elsewhere |
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 |
D8481 | Immunodeficiency due to conditions classified elsewhere |
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 |
I462 | Cardiac arrest due to underlying cardiac condition |
I468 | Cardiac arrest due to other underlying condition |
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 |
D8481 | Immunodeficiency due to conditions classified elsewhere |
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 |
I462 | Cardiac arrest due to underlying cardiac condition |
I468 | Cardiac arrest due to other underlying condition |
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 6221 | |
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 |
D8481 | Immunodeficiency due to conditions classified elsewhere |
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 6222 | |
D800 | Hereditary hypogammaglobulinemia |
D801 | Nonfamilial hypogammaglobulinemia |
D802 | Selective deficiency of immunoglobulin A [IgA] |
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 |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |