PDX Collection 6276 (continued) |
J676 | Maple-bark-stripper's lung |
J677 | Air conditioner and humidifier lung |
J678 | Hypersensitivity pneumonitis due to other organic dusts |
J679 | Hypersensitivity pneumonitis due to unspecified organic dust |
J680 | Bronchitis and pneumonitis due to chemicals, gases, fumes and vapors |
J681 | Pulmonary edema due to chemicals, gases, fumes and vapors |
J682 | Upper respiratory inflammation due to chemicals, gases, fumes and vapors, not elsewhere classified |
J683 | Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors |
J684 | Chronic respiratory conditions due to chemicals, gases, fumes and vapors |
J688 | Other respiratory conditions due to chemicals, gases, fumes and vapors |
J689 | Unspecified respiratory condition due to chemicals, gases, fumes and vapors |
J690 | Pneumonitis due to inhalation of food and vomit |
J691 | Pneumonitis due to inhalation of oils and essences |
J698 | Pneumonitis due to inhalation of other solids and liquids |
J700 | Acute pulmonary manifestations due to radiation |
J701 | Chronic and other pulmonary manifestations due to radiation |
J702 | Acute drug-induced interstitial lung disorders |
J703 | Chronic drug-induced interstitial lung disorders |
J704 | Drug-induced interstitial lung disorders, unspecified |
J708 | Respiratory conditions due to other specified external agents |
J709 | Respiratory conditions due to unspecified external agent |
J984 | Other disorders of lung |
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 |
Q334 | Congenital bronchiectasis |
R911 | Solitary pulmonary nodule |
|
PDX Collection 6277 |
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 6278 |
A021 | Salmonella sepsis |
A207 | Septicemic plague |
A227 | Anthrax sepsis |
A267 | Erysipelothrix sepsis |
A327 | Listerial sepsis |
A392 | Acute meningococcemia |
A393 | Chronic meningococcemia |
A394 | Meningococcemia, unspecified |
A400 | Sepsis due to streptococcus, group A |
A401 | Sepsis due to streptococcus, group B |
A408 | Other streptococcal sepsis |
A409 | Streptococcal sepsis, unspecified |
A4101 | Sepsis due to Methicillin susceptible Staphylococcus aureus |
A4102 | Sepsis due to Methicillin resistant Staphylococcus aureus |
A411 | Sepsis due to other specified staphylococcus |
A412 | Sepsis due to unspecified staphylococcus |
A413 | Sepsis due to Hemophilus influenzae |
A414 | Sepsis due to anaerobes |
A4150 | Gram-negative sepsis, unspecified |
A4151 | Sepsis due to Escherichia coli [E. coli] |
A4152 | Sepsis due to Pseudomonas |
A4153 | Sepsis due to Serratia |
A4154 | Sepsis due to Acinetobacter baumannii |
A4159 | Other Gram-negative sepsis |
A4181 | Sepsis due to Enterococcus |
A4189 | Other specified sepsis |
A419 | Sepsis, unspecified organism |
A427 | Actinomycotic sepsis |
A482 | Nonpneumonic Legionnaires' disease [Pontiac fever] |
A483 | Toxic shock syndrome |
A484 | Brazilian purpuric fever |
A488 | Other specified bacterial diseases |
A4901 | Methicillin susceptible Staphylococcus aureus infection, unspecified site |
A4902 | Methicillin resistant Staphylococcus aureus infection, unspecified site |
A491 | Streptococcal infection, unspecified site |
A492 | Hemophilus influenzae infection, unspecified site |
A493 | Mycoplasma infection, unspecified site |
A498 | Other bacterial infections of unspecified site |
A499 | Bacterial infection, unspecified |
A5486 | Gonococcal sepsis |
B007 | Disseminated herpesviral disease |
B377 | Candidal sepsis |
B92 | Sequelae of leprosy |
B942 | Sequelae of viral hepatitis |
B948 | Sequelae of other specified infectious and parasitic diseases |
B949 | Sequelae of unspecified infectious and parasitic disease |
|
PDX Collection 6279 |
G40001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
G40009 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
G40011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
G40019 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
G40101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
G40109 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
G40111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
G40119 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
G40201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
G40209 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
G40211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
G40219 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
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 |
G9340 | Encephalopathy, unspecified |
G9341 | Metabolic encephalopathy |
G9342 | Megaloencephalic leukoencephalopathy with subcortical cysts |
G9343 | Leukoencephalopathy with calcifications and cysts |
G9344 | Adult-onset leukodystrophy with axonal spheroids |
G9349 | Other encephalopathy |
G939 | Disorder of brain, unspecified |
G969 | Disorder of central nervous system, unspecified |
G980 | Neurogenic arthritis, not elsewhere classified |
G988 | Other disorders of nervous system |
I6783 | Posterior reversible encephalopathy syndrome |
R561 | Post traumatic seizures |
|
PDX Collection 6280 |
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 6281 |
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 6282 |
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 6283 |
E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
G40001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
G40009 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
G40011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
G40019 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
G40101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
G40109 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
G40111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
G40119 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
G40201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
G40209 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
G40211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
G40219 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
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 |