PDX Collection 4866 (continued) |
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 4867 |
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] |
D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D899 | Disorder involving the immune mechanism, unspecified |
|
PDX Collection 4868 |
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 |
I471 | 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 4869 |
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] |
D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D899 | Disorder involving the immune mechanism, unspecified |
|
PDX Collection 4870 |
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 |
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] |
D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D899 | Disorder involving the immune mechanism, unspecified |
|
PDX Collection 4871 |
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 |
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] |
D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D899 | Disorder involving the immune mechanism, unspecified |
|
PDX Collection 4872 |
J22 | Unspecified acute lower respiratory infection |
J80 | Acute respiratory distress syndrome |
J9600 | Acute respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9601 | Acute respiratory failure with hypoxia |
J9602 | Acute respiratory failure with hypercapnia |
J9610 | Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9611 | Chronic respiratory failure with hypoxia |
J9612 | Chronic respiratory failure with hypercapnia |
J9620 | Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9621 | Acute and chronic respiratory failure with hypoxia |
J9622 | Acute and chronic respiratory failure with hypercapnia |
J9690 | Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia |
J9691 | Respiratory failure, unspecified with hypoxia |
J9692 | Respiratory failure, unspecified with hypercapnia |
J988 | Other specified respiratory disorders |
J989 | Respiratory disorder, unspecified |
N80B1 | Endometriosis of pleura |
N80B2 | Endometriosis of lung |
N80B31 | Superficial endometriosis of diaphragm |
N80B32 | Deep endometriosis of diaphragm |
N80B39 | Endometriosis of diaphragm, unspecified depth |
R092 | Respiratory arrest |
|
PDX Collection 4873 |
S0190XA | Unspecified open wound of unspecified part of head, initial encounter |
S0191XA | Laceration without foreign body of unspecified part of head, initial encounter |
S0192XA | Laceration with foreign body of unspecified part of head, initial encounter |
S0193XA | Puncture wound without foreign body of unspecified part of head, initial encounter |
S0194XA | Puncture wound with foreign body of unspecified part of head, initial encounter |
S0195XA | Open bite of unspecified part of head, initial encounter |
S020XXA | Fracture of vault of skull, initial encounter for closed fracture |
S020XXB | Fracture of vault of skull, initial encounter for open fracture |
S020XXS | Fracture of vault of skull, sequela |
S02101A | Fracture of base of skull, right side, initial encounter for closed fracture |
S02101B | Fracture of base of skull, right side, initial encounter for open fracture |
S02101S | Fracture of base of skull, right side, sequela |
S02102A | Fracture of base of skull, left side, initial encounter for closed fracture |
S02102B | Fracture of base of skull, left side, initial encounter for open fracture |
S02102S | Fracture of base of skull, left side, sequela |
S02109A | Fracture of base of skull, unspecified side, initial encounter for closed fracture |
S02109B | Fracture of base of skull, unspecified side, initial encounter for open fracture |
S02109S | Fracture of base of skull, unspecified side, sequela |
S02110A | Type I occipital condyle fracture, unspecified side, initial encounter for closed fracture |
S02110B | Type I occipital condyle fracture, unspecified side, initial encounter for open fracture |
S02110S | Type I occipital condyle fracture, unspecified side, sequela |
S02111A | Type II occipital condyle fracture, unspecified side, initial encounter for closed fracture |
S02111B | Type II occipital condyle fracture, unspecified side, initial encounter for open fracture |
S02111S | Type II occipital condyle fracture, unspecified side, sequela |
S02112A | Type III occipital condyle fracture, unspecified side, initial encounter for closed fracture |
S02112B | Type III occipital condyle fracture, unspecified side, initial encounter for open fracture |
S02112S | Type III occipital condyle fracture, unspecified side, sequela |
S02113A | Unspecified occipital condyle fracture, initial encounter for closed fracture |
S02113B | Unspecified occipital condyle fracture, initial encounter for open fracture |
S02113S | Unspecified occipital condyle fracture, sequela |
S02118A | Other fracture of occiput, unspecified side, initial encounter for closed fracture |
S02118B | Other fracture of occiput, unspecified side, initial encounter for open fracture |
S02118S | Other fracture of occiput, unspecified side, sequela |
S02119A | Unspecified fracture of occiput, initial encounter for closed fracture |
S02119B | Unspecified fracture of occiput, initial encounter for open fracture |
S02119S | Unspecified fracture of occiput, sequela |
S0211AA | Type I occipital condyle fracture, right side, initial encounter for closed fracture |
S0211AB | Type I occipital condyle fracture, right side, initial encounter for open fracture |
S0211AS | Type I occipital condyle fracture, right side, sequela |
S0211BA | Type I occipital condyle fracture, left side, initial encounter for closed fracture |
S0211BB | Type I occipital condyle fracture, left side, initial encounter for open fracture |
S0211BS | Type I occipital condyle fracture, left side, sequela |
S0211CA | Type II occipital condyle fracture, right side, initial encounter for closed fracture |
S0211CB | Type II occipital condyle fracture, right side, initial encounter for open fracture |
S0211CS | Type II occipital condyle fracture, right side, sequela |
S0211DA | Type II occipital condyle fracture, left side, initial encounter for closed fracture |
S0211DB | Type II occipital condyle fracture, left side, initial encounter for open fracture |
S0211DS | Type II occipital condyle fracture, left side, sequela |
S0211EA | Type III occipital condyle fracture, right side, initial encounter for closed fracture |
S0211EB | Type III occipital condyle fracture, right side, initial encounter for open fracture |
S0211ES | Type III occipital condyle fracture, right side, sequela |
S0211FA | Type III occipital condyle fracture, left side, initial encounter for closed fracture |
S0211FB | Type III occipital condyle fracture, left side, initial encounter for open fracture |
S0211FS | Type III occipital condyle fracture, left side, sequela |
S0211GA | Other fracture of occiput, right side, initial encounter for closed fracture |
S0211GB | Other fracture of occiput, right side, initial encounter for open fracture |
S0211GS | Other fracture of occiput, right side, sequela |
S0211HA | Other fracture of occiput, left side, initial encounter for closed fracture |
S0211HB | Other fracture of occiput, left side, initial encounter for open fracture |
S0211HS | Other fracture of occiput, left side, sequela |
S02121A | Fracture of orbital roof, right side, initial encounter for closed fracture |
S02121B | Fracture of orbital roof, right side, initial encounter for open fracture |
S02121S | Fracture of orbital roof, right side, sequela |
S02122A | Fracture of orbital roof, left side, initial encounter for closed fracture |
S02122B | Fracture of orbital roof, left side, initial encounter for open fracture |
S02122S | Fracture of orbital roof, left side, sequela |
S02129A | Fracture of orbital roof, unspecified side, initial encounter for closed fracture |
S02129B | Fracture of orbital roof, unspecified side, initial encounter for open fracture |
S02129S | Fracture of orbital roof, unspecified side, sequela |
S0219XA | Other fracture of base of skull, initial encounter for closed fracture |
S0219XB | Other fracture of base of skull, initial encounter for open fracture |
S0219XS | Other fracture of base of skull, sequela |
S022XXS | Fracture of nasal bones, sequela |
S0230XS | Fracture of orbital floor, unspecified side, sequela |
S0231XS | Fracture of orbital floor, right side, sequela |
S0232XS | Fracture of orbital floor, left side, sequela |
S02400S | Malar fracture, unspecified side, sequela |
S02401S | Maxillary fracture, unspecified side, sequela |
S02402S | Zygomatic fracture, unspecified side, sequela |
S0240AS | Malar fracture, right side, sequela |
S0240BS | Malar fracture, left side, sequela |
S0240CS | Maxillary fracture, right side, sequela |
S0240DS | Maxillary fracture, left side, sequela |
S0240ES | Zygomatic fracture, right side, sequela |
S0240FS | Zygomatic fracture, left side, sequela |
S02411S | LeFort I fracture, sequela |
S02412S | LeFort II fracture, sequela |
S02413S | LeFort III fracture, sequela |
S0242XS | Fracture of alveolus of maxilla, sequela |
S025XXS | Fracture of tooth (traumatic), sequela |
S02600S | Fracture of unspecified part of body of mandible, unspecified side, sequela |
S02601S | Fracture of unspecified part of body of right mandible, sequela |
S02602S | Fracture of unspecified part of body of left mandible, sequela |
S02609S | Fracture of mandible, unspecified, sequela |
S02610S | Fracture of condylar process of mandible, unspecified side, sequela |
S02611S | Fracture of condylar process of right mandible, sequela |
S02612S | Fracture of condylar process of left mandible, sequela |
S02620S | Fracture of subcondylar process of mandible, unspecified side, sequela |
S02621S | Fracture of subcondylar process of right mandible, sequela |
S02622S | Fracture of subcondylar process of left mandible, sequela |
S02630S | Fracture of coronoid process of mandible, unspecified side, sequela |
S02631S | Fracture of coronoid process of right mandible, sequela |
S02632S | Fracture of coronoid process of left mandible, sequela |
S02640S | Fracture of ramus of mandible, unspecified side, sequela |
S02641S | Fracture of ramus of right mandible, sequela |
S02642S | Fracture of ramus of left mandible, sequela |
S02650S | Fracture of angle of mandible, unspecified side, sequela |
S02651S | Fracture of angle of right mandible, sequela |
S02652S | Fracture of angle of left mandible, sequela |
S0266XS | Fracture of symphysis of mandible, sequela |
S02670S | Fracture of alveolus of mandible, unspecified side, sequela |
S02671S | Fracture of alveolus of right mandible, sequela |
S02672S | Fracture of alveolus of left mandible, sequela |
S0269XS | Fracture of mandible of other specified site, sequela |
S0280XS | Fracture of other specified skull and facial bones, unspecified side, sequela |
S0281XS | Fracture of other specified skull and facial bones, right side, sequela |
S0282XS | Fracture of other specified skull and facial bones, left side, sequela |
S02831S | Fracture of medial orbital wall, right side, sequela |
S02832S | Fracture of medial orbital wall, left side, sequela |
S02839S | Fracture of medial orbital wall, unspecified side, sequela |
S02841S | Fracture of lateral orbital wall, right side, sequela |
S02842S | Fracture of lateral orbital wall, left side, sequela |
S02849S | Fracture of lateral orbital wall, unspecified side, sequela |
S0285XS | Fracture of orbit, unspecified, sequela |
S0291XA | Unspecified fracture of skull, initial encounter for closed fracture |
S0291XB | Unspecified fracture of skull, initial encounter for open fracture |
S0291XS | Unspecified fracture of skull, sequela |
S0292XS | Unspecified fracture of facial bones, sequela |
S060X0A | Concussion without loss of consciousness, initial encounter |
S060X1A | Concussion with loss of consciousness of 30 minutes or less, initial encounter |
S060X9A | Concussion with loss of consciousness of unspecified duration, initial encounter |
S060XAA | Concussion with loss of consciousness status unknown, initial encounter |
S061X0A | Traumatic cerebral edema without loss of consciousness, initial encounter |
S061X1A | Traumatic cerebral edema with loss of consciousness of 30 minutes or less, initial encounter |
S061X2A | Traumatic cerebral edema with loss of consciousness of 31 minutes to 59 minutes, initial encounter |
S061X3A | Traumatic cerebral edema with loss of consciousness of 1 hour to 5 hours 59 minutes, initial encounter |
S061X4A | Traumatic cerebral edema with loss of consciousness of 6 hours to 24 hours, initial encounter |
S061X5A | Traumatic cerebral edema with loss of consciousness greater than 24 hours with return to pre-existing conscious level, initial encounter |
S061X6A | Traumatic cerebral edema with loss of consciousness greater than 24 hours without return to pre-existing conscious level with patient surviving, initial encounter |
S061X7A | Traumatic cerebral edema with loss of consciousness of any duration with death due to brain injury prior to regaining consciousness, initial encounter |
S061X8A | Traumatic cerebral edema with loss of consciousness of any duration with death due to other cause prior to regaining consciousness, initial encounter |